A posterior stabilized knee orthopaedic prosthesis assembly includes a tibial bearing, a primary femoral component, and a revision femoral component. Each of the primary and revision femoral components is configured to separately articulate with the tibial bearing. However, each of the primary and revision femoral components has different geometry. The primary femoral component includes a posterior cam having a posterior cam surfacing including a concave cam surface and a convex cam surface. The revision femoral component includes a posterior cam having only a convex cam surface.
A construct for fusing a joint between a proximal bone and a distal bone comprises a plate body having a proximal end, a distal end, and a longitudinal axis extending between the proximal and distal ends; a rigid joint bridge on the plate body intermediate the proximal and distal ends, the bridge separating the plate body between a proximal bone portion and a distal bone portion; a plurality of screw receiving holes extending through the proximal bone portion of the plate, the distal most pair of the holes defining a first transverse axis at an oblique angle relative the longitudinal axis; a plurality of screw receiving holes extending through the distal bone portion of the plate, the proximal most pair of the holes defining a second transverse axis at an oblique angle relative the longitudinal axis; a plurality of screws extending through the holes and attaching the plate body to the proximal and distal bones; and a joint screw traversing the joint between the first and second transverse axes.
A customized patient-specific acetabular orthopaedic surgical instrument is disclosed. A method for fabricating and using the orthopaedic surgical instrument is also disclosed. According to one aspect of the disclosure, a customized patient-specific orthopaedic instrument for facilitating implantation of an acetabular cup prosthesis in a coxal bone of a patient is disclosed. The customized patient-specific orthopaedic instrument includes a customized patient-specific acetabular reaming guide including a ring-shaped body having an inner surface defining a cylindrical passageway, and a plurality of arms extending from the ring-shaped body.
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
9.
SEMI-CONSTRAINED ANKLE PROSTHESIS HAVING A ROTATING BEARING INSERT
A semi - constrained ankle prosthesis (10) includes a tibial component (12) configured to be coupled to a surgically-prepared surface of the distal end of a tibia, and a bearing insert (16) locked to the tibial component. The bearing insert is rotative relative to the tibial component and has an articular surface (26) formed in an inferior surface (52) thereof.
A prosthesis assembly configured for use with a scapula in one embodiment includes a spherical humeral component, an elongated glenoid bearing including a first bearing surface with (i) a first spherical end portion with a first radius of curvature, (ii) a second spherical end portion with a second radius of curvature, and (iii) a central portion located between the first spherical end portion and the second spherical end portion, and a first coupling portion extending from a second bearing surface opposite the bearing surface, and a base configured to rotatably support the elongated glenoid bearing, wherein the first radius of curvature is substantially equal to the second radius of curvature and the central portion does not have a radius of curvature that is substantially equal to the second radius of curvature.
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
A pair of plate benders are provided for bending a bone plate. Each bender includes a lever arm having a first end and a second end. The first end includes a fulcrum for placement on the upper surface of the plate, and a foot insertable through the oblong screw hole to contact the lower surface of the plate. The second end includes a cut-out with a central divider. The cut-out has a length dimensioned to extend widthwise about the plate at the location of the oblong screw hole with the divider extending into the oblong screw hole for stability. The second end may also be provided with a deep slot that accommodates the thickness of the plate. In use, plate benders with such structure can be used in pairs to longitudinal bend the plate; bend the plate in plane; or twist the plate along its axis.
A61B 19/00 - Instruments, implements or accessories for surgery or diagnosis not covered by any of the groups A61B 1/00-A61B 18/00, e.g. for stereotaxis, sterile operation, luxation treatment, wound edge protectors(protective face masks A41D 13/11; surgeons' or patients' gowns or dresses A41D 13/12; devices for carrying-off, for treatment of, or for carrying-over, body liquids A61M 1/00)
A61B 19/00 - Instruments, implements or accessories for surgery or diagnosis not covered by any of the groups A61B 1/00-A61B 18/00, e.g. for stereotaxis, sterile operation, luxation treatment, wound edge protectors(protective face masks A41D 13/11; surgeons' or patients' gowns or dresses A41D 13/12; devices for carrying-off, for treatment of, or for carrying-over, body liquids A61M 1/00)
A prosthesis assembly for use with a scapula in one embodiment includes an acromion spacer unit (108), a first articulation surface on an inferior surface of the acromion spacer unit, a bone contacting surface (132) on a superior surface of the acromion spacer unit, and a bone mounting member extending sideways from the acromion spacer unit and oriented such that when the acromion spacer unit is mounted on a scapula, the acromion spacer unit is positioned at a height above the height of a midpoint (54) of a glenoid fossa of the scapula.
A prosthesis assembly for use with a scapula is disclosed. The prosthesis assembly includes a glenoid bearing support and a bearing. The glenoid bearing support includes a glenoid vault-occupying portion configured to occupy at least a portion of a glenoid vault of the scapula, the glenoid-vault occupying portion having a first coupling component. The glenoid bearing support further includes a glenoid rim replacement portion attached to the glenoid vault-occupying portion. The bearing defines a bearing surface and has a second coupling component configured to cooperate with the first coupling component to couple the bearing to the glenoid vault-occupying portion. The glenoid vault-occupying portion defines a bearing-side end portion and an opposite-side end portion. The glenoid rim replacement portion projects outwardly from the bearing-side end portion of the glenoid vault-occupying portion. The glenoid bearing support defines a bone graft receptacle.
A prosthetic trial for a joint prosthesis includes a stem having a proximal section and a distal section for implantation in a bone. A body includes a channel receiving at least the proximal section of the stem. A locking mechanism is at least partially disposed within the body. The locking mechanism is biased into a locking position in which the mechanism locks the stem within the first channel of the body. The locking mechanism is accessible outside said body to be pulled into a releasing position to unlock the stem from the body.
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A61B 17/72 - Intramedullary devices, e.g. pins or nails
21.
METHODS OF MAKING CROSSLINKED POLYMERIC MATERIAL FOR ORTHOPAEDIC IMPLANTS
A method for making a crosslinked polymeric material for use in an orthopaedic device is described. The method may include the use of one or more crosslinking enhancers to enhance the crosslinking process.
A bending tool is provided for reshaping a bone plate that is preassembled with a pair of spaced-apart threaded, cylindrical elements removably attached to the bone plate and extending above the top surface of the bone plate. The bending tool has a handle and a distal head attached to the distal end of the handle. The distal head has a cavity that is sized and shaped to fit over the pair of spaced-apart threaded, cylindrical elements. The user, while holding the bone plate, may manually apply a leverage force to the bending tool while the cavity of the distal head is fitted over the pair of spaced-apart threaded, cylindrical elements to transmit a sufficient, regionalized bending moment to the bone plate through the pair of threaded, cylindrical elements to reshape the bone plate.
A disposable single indication orthopedic trauma surgical kit has no bone plates other than a single bone plate precountoured and sized to match an anatomic shape of a portion of a bone of a patient's extremity. The single bone plate has a plurality of fastener apertures. The surgical kit also has a plurality of fasteners with heads that are dimensioned to mate with the fastener apertures. The surgical kit also has a disposable torque driver adapted to engage the fastener heads. The foregoing components are contained in a sterile sealed container.
An instrument system is provided for positioning an internal fixation prosthesis and guiding a cannulated bone drill during a surgical, radioscopic procedure for the repair of a fractured bone of a patient. The instrument system includes a target wire (180), a handle (106) formed from a radio translucent material having a target hole for guided passage of the target wire along a target axis. The target axis coincides with the intersection of a first plane and a second plane orthogonal to the first plane. The instrument system also includes a nose component (150) attached to an end of the handle and removably connectable to the prosthesis. The nose component includes an alignment sight formed from a radio-opaque material. When the prosthesis is connected to the nose component and the target wire is positioned through the target hole along the target axis, the image of the guide wire may be radioscopically viewed along a first line of sight contained in the first plane to bisect the image of the alignment device, thereby providing a first visual reference to the user for directing the first guide wire into the desired portion of the bone while holding the prosthesis in a desired position relative to the bone.
An implant includes a body configured to be implanted at least partially within a bone canal. The body has a proximal end, a longitudinal axis and a cavity located at the proximal end. The cavity is configured to mate with an insertion tool and defines a cavity axis that is not parallel to the longitudinal axis of the implant.
A61F 2/46 - Special tools for implanting artificial joints
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A61B 17/60 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements for external osteosynthesis, e.g. distractors or contractors
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
A system, apparatus, and method for determining a position of an orthopedic prosthesis includes a patient support platform, a sensor array coupled to the patient support platform, and a controller electrically coupled to the sensor array. The sensor array is configured to generate data signals in response to an output signal of a signal source(s) coupled to the orthopedic prosthesis and/or a bone of the patient. The controller is configured to determine a position of the orthopedic prosthesis and/or the bone of the patient based on the data signals.
The present invention relates to processes involving contacting articles that include titanium or titanium alloy with a solution comprising hydrochloric acid and chloride-containing compound for a time and at a temperature effective to form a plurality of indentions that, independently, have a diameter of from about 200 nm to 10 microns.
An intramedullary nail comprises longitudinal channel, a first transverse passage and a second transverse passage. A lag screw extends through the first transverse passage of the intramedullary nail. An anti-rotation shaft extends through the second transverse passage of the intramedullary nail. A cannulated lag screw lock is positioned in the intramedullary shaft and engages the lag screw. The anti-rotation shaft extends through a cross channel in the lag screw lock. A second shaft lock is positioned in the intramedullary nail with the second shaft lock engaging the anti-rotation shaft. In at least one embodiment, the lag screw lock includes a substantially cylindrical body portion rotatably connected to a threaded head portion. In at least one embodiment, the second shaft lock is provided as an end cap including a threaded upper portion and a lower post portion that extends into the lag screw lock.
An apparatus for transcutaneously transferring an amount of energy to an implantable orthopaedic device includes a primary coil. The primary coil has a resonant frequency matched to a resonant frequency of a secondary coil, which may form part of the implantable orthopaedic device. The primary coil may have an aperture configured to receive a portion of a patient's body or may include a substantially “C”-shaped core. A power circuit may be coupled with the primary coil to provide power to the coil. The apparatus may also include a wireless receiver, a measuring device, and/or a display.
An apparatus for transcutaneously transferring an amount of energy to an implantable orthopaedic device includes a primary coil. The primary coil has a resonant frequency matched to a resonant frequency of a secondary coil, which may form part of the implantable orthopaedic device. The primary coil may have an aperture configured to receive a portion of a patient's body or may include a substantially “C”-shaped core. A power circuit may be coupled with the primary coil to provide power to the coil. The apparatus may also include a wireless receiver, a measuring device, and/or a display.
An orthopaedic prosthesis includes a curved outer surface configured to abut a patient's bone when the orthopaedic prosthesis is implanted therein. The outer surface may or may not be electrically conductive. A channel is defined in the outer surface and extends from a rim of the outer surface to a location on the outer surface. One or more electrical conductors is positioned in the channel and extends outwardly from the channel at the rim of the outer surface. A switch is positioned at the first location and is configured to establish an electrical connection between the electrical conductor and the outer surface and/or another electrical conductor when the first location of the outer surface contacts the patient's bone. The switch may be embodied as an end of the electrical conductor or a more complex switch such as a push-button type switch.
A prosthetic liner includes a convex exterior surface, a concave interior surface and a rim portion connecting the interior surface and the exterior surface. The liner includes a plurality of recesses and a plurality of fingers. Each of the plurality of recesses is formed in the exterior surface of the liner without extending to the interior surface of the liner. The plurality of fingers is positioned in the plurality of recesses and each of the plurality of fingers is connected to the exterior surface and extends toward the rim portion. The plurality of fingers may be resiliently moveable in the plurality of recesses. The plurality of fingers may be integral with the exterior surface of the liner. The rim portion may define a plane into which at least one of the plurality of fingers extends.
A method for manufacturing a spherical cage. The method includes providing a wire braid and inserting a spherical ball inside the wire braid. The wire braid and spherical ball are placed inside a mold. Excess wire braid is trimmed from the mold, creating trimmed ends of the braid. The mold is heat set with the spherical ball and wire braid. The spherical ball and wire braid are removed from the ball and the spherical ball is removed from the wire braid, resulting in a spherical wire cage.
A shoulder prosthesis includes a vault-filling component defining a bearing-facing surface and having a first coupling component, the vault-filling component including (i) a vault-filling first portion defining a first part of the bearing-facing surface, and (ii) a projecting second portion projecting from the vault-filling first portion so as to define a second part of the bearing-facing surface. The vault-filling first portion and the projecting second portion define a bone space therebetween. The shoulder prosthesis further includes a bearing component defining a bearing surface and having a second coupling component configured to cooperate with the first coupling component to couple the bearing component to the vault-filling component. At least one bone attachment member positioned in the bone space. The projecting second portion of the vault-filling component further defines a scapula-facing surface.
A miller assembly for creating a cavity in a bone. The cavity has a cross section which has a generally triangular profile having a first side generally parallel with an axis of the bone and a second side forming an acute angle with the first side, and is contiguous with a pre-existing conical cavity in the bone. The miller assembly includes a cutter and a frame for carrying the cutter. The frame includes a connection portion having a longitudinal axis and a cutter mount for mounting the cutter at a first angle approximating the acute angle with respect to the longitudinal axis of the connection portion. The cutter mount extends at the first angle from the longitudinal axis of the connection portion and is configured to receive a portion of the cutter and maintain the received cutter oriented at the first angle during rotation. The frame further includes a handle configured to form a portion of a drive joint for coupling the frame to a drill, the handle having a longitudinal axis. The longitudinal axis of the handle is coincident with the longitudinal axis of the frame.
Medical implants exhibiting optimized mechanical properties, and methods of making such implants, are disclosed. That is, the implants are fabricated of a porous metal substrate and include coating integrated over various areas so as to provide some added or desirable property or functionality to the implant. In one embodiment, the implant is an acetabular implant with a coating applied to an internal, concave wear surface which is sized and configured to receive a head of a femur. Typically, the coating is a ceramic incorporated onto the desired area of the implant via electrophoretic deposition.
A low profile bone screw system includes a retainable washer and a low profile bone screw having a smooth conical head for insertion into the washer. The washer has an axial bore with a conical portion for fully seating the screw head and a smooth outer surface shaped like the head of a conventional compression bone screw head. Washer dispensing units are also provided.
A bone plate system for the internal fixation of metacarpal and phalanx fractures of the hand is provided. The plates are structured to permit independent reconfiguration of holes of the plates relative to a longitudinal axis and are configured to orient fasteners to interdigitate with holes displaced along the longitudinal axis. The plates are very thin, and a locking screw with a low profile head design is provided for use therewith. Plate shaping tools may be attached to a plate having pre-assembled guides while the plate is located on the bone to effect alteration of the plate shape in an effective and precise manner. The tools are designed such that a drill and K-wires can be inserted through the guides while the tools are coupled to the guides.
A method (10) and instrumentation (100,200,600,700,800,900) for performing a patellofemoral arthroplasty orthopaedic procedure includes coupling an ante꧀or cutting block to a femur of a patient such that the cutting blockreferences local anatomy of the femur. The ante꧀or cutting block is used to perform a number of bone cuts to establish a trochlear cavity in the femur. The trochlear cavity is formed such that a trochlear prosthesis (300) may be inset into the cavity and substantially flush with the surrounding cartilage. A finishing burring guide (600) and burr bit (700) may be used to detail the shape and/or size of the trochlear cavity. Additionally, a trochlear drill guide (900) may be used to facilitate establishing peg holes in the patient's femur to receive corresponding pegs of the trochlear prosthesis.
A periarticular bone plate for the internal fixation of a fractured, proximal tibia of a surgical patient includes a shaft member connected to a head member, a top surface, a bottom surface, a posterior edge, an anterior edge and a plurality of holes extending between the top and bottom surfaces for receiving fasteners for attaching the plate to the bone. The head member is offset relative to the shaft member in each of a frontal and sagittal planes of the proximal tibia.
An apparatus for treating a bone fracture comprises an intramedullary rod (12) extending through a first bone segment of a fractured bone. A lag screw assembly (14) extends through a first transverse aperture in the rod, while a control member (16) extends through a second transverse aperture longitudinally offset from the first aperture. The lag screw assembly includes a lag screw engaged to the second bone segment and a locking sleeve (40) mounted over a proximal portion of the lag screw. The locking sleeve defines a groove (44) aligned with the second aperture. The control member includes a distal portion penetrating the bone segments, an intermediate portion configured to engage the second aperture, and an enlarged head (65) configured to slidably engage the groove. The groove includes a terminus that contacts the head of the control member after a predetermined amount of lateral migration of the lag screw as the fracture collapses.
An external fixator system (2) includes a fixation bar (6), a fixation pin (8), and a clamp assembly (10). The clamp assembly includes a first jaw pair (14), a second jaw pair (16), and a first spring (18) insert. The first jaw pair has a first upper jaw component (20) and a first lower jaw component (22) that collectively define a first passage configured to receive the fixation bar. The second jaw pair has a second upper jaw component (26) and a second lower jaw component (28) that collectively define a second passage (30) configured to receive the fixation pin. The first spring insert is positioned within the first passage and interposed between the first upper jaw component and the first lower jaw component. Advancement of the fixation bar into the first passage causes deflection of the first spring insert.
A universal targeting apparatus (30,100) includes a generally U-shaped body (32, 102) having one end (36,104) configured to be coupled to the proximal end (18) of the intramedullary implant (10) and a mounting portion (46,112) at an opposite end of said body. An arm (34,125) is rotatably mounted to the mounting portion of the U-shaped body and includes bores (67,73,131,136) defined at its opposite ends. Each bore is arranged at a different angle to correspond to the angle (A) of a transverse aperture (14,15) in the intramedullary implant. The arm can be rotated so an appropriate one of the angled bores is aligned with the transverse aperture to serve as a guide for creating targeting holes in the bone.
A system and method for trialing a modular hip replacement system permits evaluation and replication of the anatomic anteversion rotational angle of the femur. In one embodiment, a femoral hip implant kit includes at least one distal implant and a plurality of femoral heads, each of the plurality of femoral heads having a diameter different from the diameter of the other of the plurality of femoral heads. The kit includes a proximal trial housing with a bore within the housing, the bore configured to receive a portion of the distal implant, a collet located within the bore, the collet including an outer wall portion extending between a top surface portion and a bottom surface portion, a collapsing member for engaging the portion of the distal implant and for forcing the top surface portion of the collet toward the bottom surface portion of the collet along a first axis.
An orthopaedic surgical device comprises a first sensor component and a second sensor component. Each sensor component includes a paddle set to contact a proximal tibia and a distal femur of a patient. The first sensor component and the second sensor component being movable with respect to one another to extend one paddle set beyond the other paddle set, and each paddle set includes cutouts for the clearance of the patellar tendon to avoid the need to avert the patella during use.
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
A prosthesis assembly in one embodiment includes a stem configured to be implanted in a bone and including a first coupling portion, a head having a bearing surface configured to mate with at least one of a natural opposing joint component and a prosthetic opposing joint component, the head further having a second coupling portion, a coupler including a third coupling portion and a fourth coupling portion, the third coupling portion configured to couple with the second coupling portion, and an insert including (i) a fifth coupling portion configured to couple with the fourth coupling portion in any of a plurality of rotational orientations in combination with any of a plurality of roll angles and any of a plurality of pitch angles, and (ii) a sixth coupling portion configured to couple with the first coupling portion only when the insert assumes a predetermined rotational orientation with respect to the stem.
Provided are methods for processing a green body that includes compacted metal powder, comprising impacting the green body with a particulate material for a time and under conditions effective to displace a portion of the metal powder from the green body. The present methods can be used to prepare green bodies that have "roughened" surfaces and that can be used to make orthopedic implants displaying low movement relative to bone when installed in situ, which corresponds to higher stability upon implantation and decreases the time required for biological fixation of the implant. Also provided are implants comprising a metallic matrix, and methods comprising surgically installing an implant prepared from a "surface roughened" green body in accordance with the present invention.
B22F 3/00 - Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sinteringApparatus specially adapted therefor
B22F 5/00 - Manufacture of workpieces or articles from metallic powder characterised by the special shape of the product
B22F 3/04 - Compacting only by applying fluid pressure
An instrument for use in resecting a portion of a greater tubercle of a humerus in shoulder arthroplasty is provided. The instrument includes a guide support that has a first end coupled to a long bone. The guide support extends laterally and over the greater tubercle. The instrument also includes a cutting guide movably coupled to the guide support. The cutting guide including curved frame for abutting the humerus.
A bone cutting assembly includes a guide pin that may be securely inserted into a bone to define a cutting axis. The bone cutting assembly also includes a housing having a cam surface and features for temporarily fastening the housing to the bone. The bone cutting assembly also includes a burr mounting arm that rotatably and slidably fits onto the guide pin so that the arm can swing around the cutting axis and also translate up and down the guide pin. A user may move the burr mounting arm about the cutting axis so that the arm follows along the cam surface of the housing.
A nail assembly (100) for use in trauma surgery is provided. The nail assembly includes an intramedullary shaft (102) including a first transverse passage (104) and a second transverse passage (106) in the shaft. The,.first transverse passage and the second transverse passage do not contact each other on the shaft. The nail assembly also includes a first shaft (112) extending through the first transverse passage in the intramedullary shaft and a second shaft (114) extending through the second transverse passage in the intramedullary shaft. The second shaft includes an engagement feature (116) configured to bring the second shaft into contact with the first shaft. The engagement feature may be in the form of a lateral mechanical feature that provides simultaneous unilateral coupled motion of the first shaft with the second shaft through the transverse passages in the intramedullary shaft.
A cutting guide for removal of bone during arthroplasty. The cutting guide includes a housing having a three-dimensional guide path and an arm coupled to the housing and extending through the guide path. The arm includes a burr. As the arm is slid along the path, the burr simultaneously cuts in two planes on the bone.
A drill sleeve is provided for guiding a bone drill in alignment with the screw holes and drill guides. The drill sleeve includes a cylindrical body having a first end, a second end and a longitudinal axis extending therebetween. The cylindrical body includes a longitudinal bore therethrough that is sized for passage of a bone drill. The drill sleeve also includes a frictional retaining element for exerting a bearing force against the surface of the bone drill, such that the frictional retaining element may support at least the weight of the drill sleeve on the bone drill. The bone drill has graduated indicia, and a portion of the drill sleeve may be referenced relative to the indicia so as to be used as a depth gauge for determining the length of a drilled hole in order to select a screw fastener having the appropriate length.
A61B 17/88 - Methods or means for implanting or extracting internal fixation devices
A61B 19/00 - Instruments, implements or accessories for surgery or diagnosis not covered by any of the groups A61B 1/00-A61B 18/00, e.g. for stereotaxis, sterile operation, luxation treatment, wound edge protectors(protective face masks A41D 13/11; surgeons' or patients' gowns or dresses A41D 13/12; devices for carrying-off, for treatment of, or for carrying-over, body liquids A61M 1/00)
A magnetic sensor array includes a first three-dimensional magnetic sensor secured to a substrate in a central location of the substrate. A number of second three-dimensional magnetic sensors are secured to the substrate at a first distance from the first magnetic sensor. Additionally, a number of one-dimensional magnetic sensors are secured to the substrate at a second distance from the first magnetic sensor greater than the first distance. Additional magnetic sensors of any dimension may also be included. The magnetic field sensitivity of the first and second three-dimensional magnetic sensors may be less than the magnetic field sensitivity of the one-dimensional magnetic sensors. The sensing range of the first and second three-dimensional magnetic sensors may be greater than the sensing range of the one-dimensional magnetic sensors. The magnetic sensor array may also include a processing circuit coupled to the magnetic sensors.
G01R 33/02 - Measuring direction or magnitude of magnetic fields or magnetic flux
G01B 7/14 - Measuring arrangements characterised by the use of electric or magnetic techniques for measuring distance or clearance between spaced objects or spaced apertures
54.
Method and system for fabricating an aspherical orthopaedic prosthetic component
A method and apparatus for fabricating an aspherical orthopaedic prosthetic component includes rotating the orthopaedic prosthetic component and operating an electrical discharge machining cutting tool (EDM) to move a wire electrode of the EDM along a number of arcuate cutting paths. A spark is generated between the wire electrode and the orthopaedic prosthetic component to remove a portion of the orthopaedic prosthetic component.
A method and apparatus for fabricating an orthopaedic prosthetic component includes rotating the orthopaedic prosthetic component and operating an electrical discharge machining cutting tool (EDM) to move a wire electrode of the EDM along an arcuate path. A spark is generated between the wire electrode and the orthopaedic prosthetic component to remove a portion of the orthopaedic prosthetic component.
A distal tibia plating system includes anterolateral (10) and medial plates (110). The anterolateral plate includes a shaft (12) with both threaded first fastener holes (24) and compression slots (26) along its length. The head includes a first row of four threaded fastener holes arranged transversely to the longitudinal axis, a non- threaded compression screw hole, and a plurality of distal tabs (38). Each tab includes a ring (38) with a single threaded fastener hole and a bridge (50) that couples the ring to the distal end of the plate. The bridge is configured to bend preferentially in a desired direction and to allow tab removal. The medial plate (110) is a low profile plate including a shaft (112) and a relatively enlarged distal head (116). Several fasteners (500) can be used with the plates. A plate holder (400) is provided to maneuver the plates subcutaneously.
A system for the internal fixation of a fractured bone of an elbow joint of a patient includes at least one bone plate, each bone plate having a plurality of holes and generally configured to fit an anatomical surface of the fractured bone. The at least one plate is adapted to be customized to the shape of a patient's bone. The system also includes a plurality of fasteners including at least one locking fastener for attaching the bone plate to the bone. At least one of the holes is a threaded hole. Guides for plate benders, drills, and/or K-wires can be pre-assembled to the threaded holes, and the locking fastener can lock into any of the threaded holes after the guides are removed.
An instrument for use in implanting a joint prosthesis into a bone. The instrument includes a rod having a proximal end and a distal end, the proximal end includes a visual indicator. The instrument also includes a housing, such that the rod is moveable in a longitudinal direction relative to the housing. The visual indicator is capable of emitting light when the instrument is in use. As the rod moves in the longitudinal direction, the visual indicator enters into the housing, causing the light emitted to disappear.
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A61B 17/00 - Surgical instruments, devices or methods
A61B 18/18 - Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves
An intramedullary nail for use in a medullary canal of an epiphysis and a diaphysis of a long bone is provided. The nail includes a body (106) having a length in a longitudinal direction and a width in the transverse direction normal to the longitudinal direction. The body has a diaphyseal portion and a first epiphyseal portion. The diaphyseal portion has an external periphery configured for placement in the medullary canal of the diaphysis of the long bone. The diaphyseal portion defines a longitudinally extending first surface of the diaphyseal portion. The first surface defines a longitudinally extending first void (108). The first epiphyseal portion extends from the diaphyseal portion. The first epiphyseal portion is configured for placement in the medullary canal of the first epiphysis of the long bone. The nail also includes a first insert (110) positioned in the longitudinally extending first void of the diaphyseal portion. The first insert and the diaphyseal portion of the body are made from different materials.
A customized patient-specific orthopaedic instrument, comprising : a customized patient-specific femoral cutting block (1300) that comprises : (i) a body (1302) having a bone-facing surface (1312) having a customized patient-specific negative contour (1328) configured to receive a portion of an anterior side of a patient's femur that has a corresponding positive contour; (ii) at least one tab extending posteriorly form the body, the at least one tab (1304, 1306) having a bone-facing surface having a customized patient-specific negative contour configured to receive a portion of the distal side of the patient's femur that has a corresponding positive contour; and (iii) a lip (1308, 1310) extending superiorly from an end of the at least one tab, the lip having a bone-facing surface having a customized patient-specific negative contour configured to receive a portion of the posterior side of the patient's femur that has a corresponding positive contour. A number of orthopaedic surgical instruments are also disclosed. A method, apparatus, and system for fabricating such instruments are also disclosed.
Systems, methods, and devices are disclosed which generate surgical plans that have been customized for a particular patient. One such system includes a client, a surgical plan system and a computer assisted orthopaedic surgery system. The client generates a surgical plan request that includes data relevant to a patient and an orthopaedic surgical procedure to be performed upon the patient. The surgical plan system receives the surgical plan request and generates a surgical plan that has been customized based upon the data of the surgical plan request. The computer assisted orthopaedic surgery system assists a surgeon performing the orthopaedic surgical procedure per the surgical plan generated by the surgical plan system.
G06Q 50/00 - Information and communication technology [ICT] specially adapted for implementation of business processes of specific business sectors, e.g. utilities or tourism
A61B 17/88 - Methods or means for implanting or extracting internal fixation devices
A61B 19/00 - Instruments, implements or accessories for surgery or diagnosis not covered by any of the groups A61B 1/00-A61B 18/00, e.g. for stereotaxis, sterile operation, luxation treatment, wound edge protectors(protective face masks A41D 13/11; surgeons' or patients' gowns or dresses A41D 13/12; devices for carrying-off, for treatment of, or for carrying-over, body liquids A61M 1/00)
A modular bone plating system in one embodiment is a bone plate kit including a plurality of bone plates (100, 200, 300), each of the plurality of bone plates including a male coupling portion (108, 202), a female coupling portion (110, 302) and a shaft (102, 312) extending between the male coupling portion and the female coupling portion, wherein each of the male coupling portions of each of the plurality of bone plates is configured to couple with each of the female coupling portions of each of the other of the plurality of bone plates.
A polyaxial locking screw system includes a bone plate defining a plate hole with an inner spherical surface and a relatively harder split polyaxial bushing with a outer spherical surface provided within the plate hole for receiving a bone screw. In one embodiment, the plate is formed from titanium alloy, while the bushing is formed from a cobalt chrome alloy. The outer surface of the polyaxial bushing includes a plurality of spikes. When the screw is inserted into the bushing, since the bushing material is considerably harder than the plate material, the forceful expansion of the bushing during screw insertion causes the spikes to penetrate into the inner spherical surface of the hole, thereby increasing the frictional engagement of the bushing to the plate to lock the screw at a desired angle.
The invention provides a medical implant device or component thereof comprising a metal substrate, an intermediate coating, and an outer coating of aluminum oxide, as well as a method of making such a medical implant device or component thereof.
B05D 3/02 - Pretreatment of surfaces to which liquids or other fluent materials are to be appliedAfter-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by baking
A tibial tray assembly includes a platform having a stem extending downwardly from a bottom surface and a stem extension couple to the an end of the stem. The stem extension is electrically insulated from the stem. The tibial tray assembly also includes a wireless communication device configured to transmit data using the stem extension as an antenna.
An apparatus for transcutaneously transferring an amount of energy to an implantable orthopaedic device includes a primary coil. The primary coil has a resonant frequency matched to a resonant frequency of a secondary coil, which may form part of the implantable orthopaedic device. The primary coil may have an aperture configured to receive a portion of a patient's body or may include a substantially “C”-shaped core. A power circuit may be coupled with the primary coil to provide power to the coil. The apparatus may also include a wireless receiver, a measuring device, and/or a display.
The present invention concerns articles having an outer surface that bears at least two layers of metal particles, wherein the at least two layers comprise an outermost layer and an intermediate layer; the outermost layer consisting essentially of aspherical metallic particles having a mean particle size of 50 to 500 microns; and the intermediate layer consisting essentially of substantially spherical metallic particles having a mean particle size of from 50 to 500 microns. In some embodiments, the outer surface has a volume porosity of between about 20% to about 80%.
The invention provides a hydrogel composition comprising water and a hydrophilic polymer, wherein the hydrogel composition has (a) an ultimate tensile strength of about 10 kPa or more, (b) a compressive strength of about 70 kPa or more, or (c) an ultimate tensile strength of about 10 kPa or more and a compressive strength of about 70 kPa or more. The invention further provides methods for producing a hydrogel composition.
A first articulating member for use with a second articulating member to form a prosthesis for use in joint arthroplasty for a joint formed between adjacent first and second bones in which a bone fragment having an exterior surface has separated from the first bone is provided. The first articulating member includes an articulating portion having an articulation surface for articulation with the second articulating member and an attaching portion connected to the articulating portion for attachment to the first bone. The first articulating member also includes a fragment portion connected to at least one of the articulating portion and the insertion portion. The fragment portion includes a surface for contact with the external periphery of the bone fragment.
A kit for removing calcar bone from a resected face around a bone canal of a long bone prepared to receive an orthopaedic implant is provided. The kit includes a trial for insertion into the bone canal of the long bone and a fixture. The fixture has a connector for connecting the fixture to the trial and a guide for guiding the calcar reamer. The kit also includes a calcar reamer for removing calcar bone from the resected face around the bone canal of the long bone. The reamer includes a feature for cooperation with the guide of the fixture. The kit further includes an implant for insertion into the bone canal of the long bone.
A61B 17/00 - Surgical instruments, devices or methods
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A61F 5/00 - Orthopaedic methods or devices for non-surgical treatment of bones or jointsNursing devices
74.
Method and system for registering a bone of a patient with a computer assisted orthopaedic surgery system
A method and system for registering a bone of a patient with a computer assisted orthopaedic surgery system includes retrieving an image of the bone having indicia of the position of a magnetic source coupled thereto, determining first data indicative of the position of the magnetic source in a bone coordinate system, determining second data indicative of a correlation between a coordinate system of the image and the bone coordinate system based on the first data; and displaying an image of the bone based on the second data.
A glenoid component apparatus for shoulder arthroplasty includes a bearing portion and a stem portion connected to the bearing portion. The stem portion is modeled from a normalized glenoid vault morphology. A method for making a glenoid component for shoulder arthroplasty includes obtaining a model of a normalized glenoid vault morphology and producing a stem portion of the glenoid component based on the model.
A system and method for trialing a modular hip replacement system permits evaluation and replication of the anatomic anteversion rotational angle of the femur. In one embodiment, a femoral hip implant kit includes at least one distal implant and a plurality of femoral heads, each of the plurality of femoral heads having a diameter different from the diameter of the other of the plurality of femoral heads. The kit includes a proximal trial housing with a bore within the housing, the bore configured to receive a portion of the distal implant, a collet located within the bore, the collet including an outer wall portion extending between a top surface portion and a bottom surface portion, a collapsing member for engaging the portion of the distal implant and for forcing the top surface portion of the collet toward the bottom surface portion of the collet along a first axis.
A system, apparatus, and method for determining a position of an orthopaedic prosthesis includes a patient support platform, a sensor array coupled to the patient support platform, and a controller electrically coupled to the sensor array. The sensor array is configured to generate data signals in response to an output signal of a signal source(s) coupled to the orthopaedic prosthesis and/or a bone of the patient. The controller is configured to determine a position of the orthopaedic prosthesis and/or the bone of the patient based on the data signals.
A modular femoral joint prosthesis includes a femoral component having a post extending therefrom, a femoral stem, and a femoral sleeve configured to be coupled to the post of the femoral assembly and to the femoral stem. The femoral sleeve is bowed posteriorly in the sagittal plane.
A prosthetic knee system includes a tibial tray (4012), a non- rotating tibial insert (4014), and a rotating tibial insert (4016). The non-rotating tibial insert and the rotating tibial insert are selectively couplable to the tibial tray such that a fixed or a mobile orthopaedic prosthesis may be configured. In some embodiments, the tibial tray may be a fixed or mobile tibial tray. Additionally, in some embodiments, the prosthetic knee system may include a femoral component.
A prosthetic knee system includes a tibial tray (512), a non-rotating tibial insert (514), and a rotating tibial insert (16). The non-rotating tibial insert and the rotating tibial insert are selectively couplable to the tibial tray such that a fixed or a mobile orthopaedic prosthesis may be configured. In some embodiments, the tibial tray may be a fixed or mobile tibial tray. Additionally, in some embodiments, the prosthetic knee system may include a femoral component.
A prosthetic knee system includes a tibial tray (212), a non-rotating tibial insert (214), and a rotating tibial insert (272). The non- rotating tibial insert and the rotating tibial insert are selectively couplable to the tibial tray such that a fixed or a mobile orthopaedic prosthesis may be configured. In some embodiments, the tibial tray may be a fixed or mobile tibial tray. Additionally, in some embodiments, the prosthetic knee system may include a femoral component.
A prosthetic knee system includes a tibial tray (4802), a non-rotating tibial insert, and a rotating tibial insert. The non- rotating tibial insert and the rotating tibial insert are selectively coupleable to the tibial tray such that a fixed or a mobile orthopaedic prosthesis may be configured. In some embodiments, the tibial tray may be a fixed or mobile tibial tray. Additionally, in some embodiments, the prosthetic knee system may include a femoral component. The tibial tray includes a platform (4806) having a guide track (4812) extending downwardly from the bottom surface (4810). A stem (4804) is coupled to the tibial tray via a mounting end (4824) received in the guide track.
A prosthetic knee system includes a tibial tray (12), a non- rotating tibial insert (14), and a rotating tibial insert (16). The non-rotating tibial insert and the rotating tibial insert are selectively couplable to the tibial tray such that a fixed or a mobile orthopaedic prosthesis may be configured. In some embodiments, the tibial tray may be a fixed or mobile tibial tray. Additionally, in some embodiments, the prosthetic knee system may include a femoral component.
A fracture fixation plate system for use on a long bone having a metaphysis and a diaphysis, includes at least one end plate having a head portion for the metaphysis, and at least one diaphyseal plate having a first end and a second end with a plurality of screw holes therebetween. The end plate includes mating structure adapted to mate with and securely couple to at least one end of the at least one diaphyseal plate. The system preferably includes several end plates and diaphyseal plates to accommodate anatomy of various sizes.
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
85.
Orthopaedic component manufacturing method and equipment
A method of reducing the surface roughness of articulating surfaces of orthopaedic implants is provided. The method includes the steps of providing an abrasive particle providing a chemical including at least one of an oxidant, a corrosion inhibitor, a complexing agent and a surfactant, combining the chemical with the abrasive particle to form a slurry, and polishing the implant with the slurry.
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
87.
Bearing material of medical implant and methods for making it
Disclosed is a bearing material of a medical implant, which is an ultrahigh molecular weight polyethylene (UHMWPE) composite. The composite comprises, for example, UHMWPE and a polyethylene copolymer having a polymer backbone and pendant hydrophilic groups or pendant surface active agents that are attached to the polymer backbone. Also disclosed are methods for preparing bearing materials. The bearing material has one or more advantageous properties including reduced immune response, reduced wear, and/or increased lubrication.
C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bondsCompositions of derivatives of such polymers
C08L 29/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radicalCompositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acidsCompositions of derivatives of such polymers
C08L 33/02 - Homopolymers or copolymers of acidsMetal or ammonium salts thereof
C08L 35/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereofCompositions of derivatives of such polymers
B28B 19/00 - Machines or methods for applying the material to surfaces to form a permanent layer thereon
88.
Registration pointer and method for registering a bone of a patient to a computer assisted orthopaedic surgery system
A registration pointer includes a camera located in an elongated shaft having a distal end configured to be contacted to a bone of a patient to register the bone to a computer assisted orthopaedic surgery system. The camera may be a hemispherical camera and may include a panoramic camera and a wide-angle camera equipped with a fish-eye lens. The registration pointer is configured to transmit images received by the cameras to the computer assisted orthopaedic surgery system for display thereon. The computer assisted orthopaedic surgery system may be configured to generate an image, such as a hemispherical image, based on the images received from the registration pointer.
Disclosed is a bearing material of a medical implant comprising a polymer such as UHMWPE and a surface active agent that is not covalently bonded to the polymer. The bearing material has a reduced wear rate. Also disclosed is a method of reducing the wear rate of a polymeric bearing material of a medical implant when it articulates against a hard counterface in the presence of synovial fluid, the method comprising providing a surface active agent in the synovial fluid in close proximity to the bearing surface, the hard counterface, or both.
A bone fixation system includes a plate and a set of fixation locking screws. The plate defines a set of locking screw holes each having an internal thread. Each respective locking screw has a head with an external structure that is adapted to self-tap into the internal thread of a given locking screw hole to secure the respective first-type fixation locking screw at an surgeon- directed angle relative to the plate. This angle is defined during forcible insertion and rotation of the respective locking screw into the given screw hole. The system may also include unidirectional locking screws. In a preferred embodiment the plate and first-type of screw are made of different metals, with the plate made of titanium alloy and the screw made of cobalt chrome alloy.
A humeral fracture fixation system is provided and includes a nail-plate fixation device having a plate-like head portion, an intramedullary nail portion, and a bent neck portion therebetween which creates an angle between the plate and nail portions. The upper surface of the nail portion is substantially straight for contact with the endosteum and the nail portion includes threaded holes for machine screws. The head portion includes locking holes for receiving fixed-angle bone support elements, and K- wire alignment holes. The front of the head portion includes suture holes while presenting a smooth profile. A specific implantation jigs and a screw guide cannula are also provided.
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A fracture fixation plate system for use on a long bone having a metaphysis and a diaphysis, includes at least one end plate having a head portion for the metaphysis, and at least one fragment plate having a first end and a second end with a plurality of screw holes therebetween. The end plate includes mating structure adapted to mate with and securely couple to at least one end of the at least one fragment plate. The system preferably includes several end plates and fragment plates to accommodate anatomy of various sizes.
A61B 17/56 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A fracture fixation device includes a plate portion and an intramedullary nail portion which is offset relative to the plate portion by a neck portion. The plate portion includes longitudinally displaced peg holes which orient pegs along an imaginary surface parallel to subchondral bone of an articular surface. The upper surface of the plate portion includes a dimple to reference a jig. The nail portion includes threaded screw holes oriented normal to an endosteal surface, and a smaller K- wire alignment hole parallel to the screw holes. The jig has a first portion which references with the dimple and a second portion in alignment over the screw holes of the nail portion. The back of the first portion of the jig is curved upward to facilitate maneuvering of the jig. The first and second portions of the jig includes K-wire guide holes which direct K-wires relative to holes in the device.
A61B 17/56 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A magnetic sensor array includes a first three-dimensional magnetic sensor secured to a substrate in a central location of the substrate. A number of second three-dimensional magnetic sensors are secured to the substrate at a first distance from the first magnetic sensor. Additionally, a number of one-dimensional magnetic sensors are secured to the substrate at a second distance from the first magnetic sensor greater than the first distance. Additional magnetic sensors of any dimension may also be included. The magnetic field sensitivity of the first and second three-dimensional magnetic sensors may be less than the magnetic field sensitivity of the one-dimensional magnetic sensors. The sensing range of the first and second three-dimensional magnetic sensors may be greater than the sensing range of the one-dimensional magnetic sensors. The magnetic sensor array may also include a processing circuit coupled to the magnetic sensors.
G01R 33/02 - Measuring direction or magnitude of magnetic fields or magnetic flux
G01B 7/14 - Measuring arrangements characterised by the use of electric or magnetic techniques for measuring distance or clearance between spaced objects or spaced apertures
95.
Orthopaedic component manufacturing method and equipment
A system for use in preparing an articulating surface of a component of an orthopaedic implant is provided. The system includes a magnetorheological polishing fluid including a carrier fluid and a plurality of particles suspendable in said carrier fluid. The system also includes a vessel for containing the Magnetorheological polishing fluid. The system also includes a mechanism for delivering the fluid to form a polishing zone and a holder for securing the component and for moveably positioning the articulating surface of the component relative to the polishing zone. The system further includes a controller for determining the rate of material removal from the object, for determining the direction and velocity of movement of the polishing zone relative to the object and for determining the number of cycles of polishing required.
B24B 49/00 - Measuring or gauging equipment for controlling the feed movement of the grinding tool or workArrangements of indicating or measuring equipment, e.g. for indicating the start of the grinding operation
96.
MODULAR FIXED AND MOBILE BEARING PROSTHESIS SYSTEM
A knee prosthetic system includes a femoral component, a fixed tibial bearing component, a mobile tibial bearing component and an integrated or common tibial base component. The same tibial base component can be used with either the fixed tibial bearing component or the mobile tibial bearing component. The fixed bearing component and tibial base component have mating anti-rotation features. One embodiment of the mobile bearing component does not engage the anti-rotation feature of the tibial base component. Another embodiment engages the anti-rotation feature to allow for limited rotation.
A fracture fixation system includes a plate having a first suture anchor location having an opening at the upper surface of the plate, an opening at the proximal end of the plate, and an opening at the anterior side of the plate and defines first and second suture pathways which cross within the plate. The first and second suture pathways include a common opening. A second suture anchor location on the plate has an opening at the upper surface of the plate, an opening at the proximal end of the plate, and an opening at the posterior side of the plate which defines third and fourth suture pathways which cross within the plate. The third and fourth suture pathways also share a common opening. Thus, each suture anchor location is capable of providing a hold for suture from multiple approaches to secure tuberosities relative to the plate.
A tool for separating components of a modular prosthesis includes an upper and lower body, each defining opposing bills at one end that are sized to fit in juxtaposed relation within an initial gap between the components. The upper body is provided with a handle so that the tool may be manually held by the surgeon with the opposing bills in position in the prosthesis. The tool includes a jack assembly disposed between the upper and lower bodies of the tool that is configured to be driven into an extended position, gradually separating the upper and lower bodies, and consequently exerting a separation force on the prosthesis components through the bills of the tool. The jack assembly is driven by a threaded actuator rod that bears against one element of the jack assembly as the actuator rod is rotated within a threaded bore in one of the bodies of the tool.
Disclosed is a polymeric orthopaedic bearing material for use as an implant material or part thereof comprising one or more crosslinked regions and one or more non-crosslinked or substantially non-crosslinked regions at the surface. The bearing material can be prepared from a crosslinkable polymer, e.g., ultrahigh molecular weight polyethylene. The orthopaedic bearing material has an advantageous combination of at least one wear property and at least one mechanical property. Also disclosed are processes for producing orthopaedic bearing materials, for example, by irradiating a raw material in consolidated form through a radiation mask having a perforated pattern for crosslinking selected regions of the raw material, and optionally shaping the raw material into a bearing material. Alternatively, a pulsed radiation beam can be used for crosslinking.
An extraction device for removing a liner from an acetabular cup is provided. The extraction device includes a jaw and a handle. The jaw is for cooperation with the liner and including a portion of the jaw for penetrating into the liner. The handle is operably associated with the jaw and is adapted for gripping the extraction device.
A61B 17/58 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements
A61B 17/60 - Surgical instruments or methods for treatment of bones or jointsDevices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements for external osteosynthesis, e.g. distractors or contractors
A61F 2/00 - Filters implantable into blood vesselsProstheses, i.e. artificial substitutes or replacements for parts of the bodyAppliances for connecting them with the bodyDevices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
patents
