Abstract: An acetabular shell liner for use in a hip arthroplasty surgical procedure is disclosed. The acetabular shell liner includes a semi-hemispherical inner bearing layer, which includes a rim and a dome attached to the rim. The semi-hemispherical inner bearing layer includes a polymeric material having a first thickness, at an apex of the dome, and a second thickness, at the rim, that is less than the first thickness. Additionally, the acetabular shell liner includes a semi-hemispherical outer reinforcement layer mated with and encasing the dome of the semi-hemispherical inner bearing layer. The semi-hemispherical outer reinforcement layer includes a metallic material to provide structural support to the semi-hemispherical inner bearing layer.

Abstract: An acetabular liner having a closed first end, an open second end, and a liner wall having a distal peripheral edge. The acetabular liner wall can include an interior surface, an exterior surface configured to be received within an acetabular shell, a first cutout through the liner wall, a second cutout parallel to the first cutout and through the liner wall, and a third cutout in the interior surface partially through the liner wall, the third cutout extending between the first and second cutouts, and at least one movable tab extending from the peripheral edge inwardly towards an axial center of the liner and having sidewalls defined by one of the sets of cutouts, the tab comprising at least one projection on an exterior surface of the tab configured to removably secure to a portion of an acetabular shell.

Abstract: The present disclosure provides a method for surface modification of a titanium implant material and a titanium implant obtained by the method for surface treatments. A titanium implant according to one embodiment of the present disclosure has high bond strength between implant and bone and its corrosion resistance.

Abstract: Implant assemblies for reverse shoulder arthroplasty are disclosed. In one embodiment, the implant assembly comprises a humeral component, an adaptor fixed to the neck of the humeral component, and a glenosphere bearing component coupled to the adaptor. The glenosphere bearing component comprises a first bearing surface that interfaces with an articulating surface of the adaptor to allow the adaptor to rotate relative to the adaptor and humeral component. The adaptor and the glenosphere bearing component form a locking mechanism that prevents the adaptor from decoupling from the glenosphere bearing component while allowing the adaptor to remain rotatable relative to the glenosphere bearing component after the implant assembly is implanted in the patient The second bearing surface is configured to interface with a glenosphere component to allow the glenosphere bearing component to articulate relative to the glenosphere component.

Abstract: Embodiments of the invention described herein thus provide implants and methods for manufacturing an implant having an outer layer that is porous. The porous outer layer can help encourage tissue ingrowth into the implant. The porous outer layer may be positioned around a core structure this is solid or that has a hollow interior. The core structure may be spherical or any other appropriate shape for a medical implant.

Abstract: A method for assessing the orthopaedic performance of a joint of a patient can comprise implanting at least a first and second RF wirelessly detectable markers in first and second bones associated with a site and determining and storing their positions before a surgical procedure is performed. The procedure can be carried out on the site and the positions of the first and second markers can be detected and stored after the procedure has been completed. The detected positions can be used to generate a representation of the orthopaedic performance of the joint after the procedure.

Abstract: In one embodiment, the present disclosure relates to an acetabular cup for implantation into a prepared acetabulum. The acetabular cup includes an inner surface, an outer surface, and an end face that separates the inner surface and the outer surface. The end face is opposite a polar region of the acetabular cup and circumscribes an open end of the acetabular cup. A plurality of protrusions project outwardly from the outer surface at predefined locations. The acetabular cup is operatively engaged to the prepared acetabulum in a planned orientation when the plurality of protrusions are received in corresponding predefined recesses in the prepared acetabulum.

Abstract: An acetabular prosthesis assembly includes an acetabular shell component and an acetabular bearing component. The shell component includes a concave inner wall having a tapered surface with multiple anti-rotation slots defined therein. The bearing component includes a convex outer wall as well as an annular flange and multiple anti-rotation keys extending radially outward from the outer wall. When the anti-rotation keys are positioned in rotational alignment with the anti-rotation slots, the flange of the bearing component is positioned in contact with the tapered surface of the shell component. When the anti-rotation keys are positioned out of rotational alignment with the anti-rotation slots, the flange is spaced apart from the tapered surface. Methods for assembling and using the acetabular prosthesis assembly are also disclosed.

Abstract: An implant injection system and method for introducing a bone implant material into a patient's bone to serve as an anchor or to fill a void in the bone. The system and method provide a quantity of meltable material which is melted in situ so that the melted material can flow and diffuse into, and be anchored to, the cancellous bone portion beneath the cortical bone layer. The flowing of the bone implant material can be accomplished by a heater located at the distal end of the implant injection system. The implant material may be provided in multiple layers with an inner layer having a lower flowing temperature than the outer layers. There can also be a looped suture that passes though the meltable material, with the free ends of the suture extending outwardly to be tied to soft tissue to affix the soft tissue to the bone.

Abstract: A method comprising cutting a channel through a femoral neck and into a femoral head of a femur, and inserting a femoral implant within the channel such that a porous portion of the femoral implant is positioned within the femoral head and a resorbable portion of the femoral implant is positioned within the femoral neck, the porous portion being coupled to the resorbable portion and extending therefrom along a longitudinal axis of the femoral implant, the resorbable portion having a cross-sectional area defined in a plane extending transverse to a longitudinal axis of the femoral implant, the cross-sectional area of the resorbable portion consisting essentially of a resorbable material.

Abstract: A hinge knee system includes a tibial assembly having a baseplate component and an axle component. The baseplate component has an opening that extends therein from a proximal end toward a distal end thereof. The axle component has a shaft portion receivable within the opening of the baseplate component and an axle connected to the shaft portion that extends in a direction transverse to a longitudinal axis of the shaft portion. The system also includes a femoral assembly that includes a distal femoral component. The distal femoral component includes condylar portions and an intercondylar portion disposed between the condylar portions. The intercondylar portion includes a bearing surface that defines a recess configured to rotatably receive the axle for articulation therewith.

Abstract: Implantable medical devices are provided. In one embodiment, a device includes a body having an external surface defining an outer profile of the device. The body includes a porous matrix including a series of interconnected macropores defined by a plurality of interconnected struts each including a hollow interior. A filler material substantially fills at least a portion of the series of interconnected macropores. The external surface of the body includes a plurality of openings communicating with the hollow interior of at least a portion of the plurality of interconnected struts. In a further aspect of this embodiment, the external surface includes exposed areas of the filler material and porous matrix in addition to the exposed openings. In another aspect, the porous matrix is formed from a bioresorbable ceramic and the filler material is a biologically stable polymeric material. Still, other aspects related to this and other embodiments are also disclosed.

Abstract: An implant system for a knee comprising a femur and a patella. The implant system includes a patella implant comprising an implant body. The implant body comprises a bone facing surface, an articular facing surface, and at least one dimple. The bone facing surface engages bone beneath an implant site formed in the patella. The articular facing surface faces towards an articulating surface of the femur and has a non-anatomical shape (such as a dome). The dimples are formed in the articular facing surface and have a load bearing surface to engage against the articulating surface of the femur. The load bearing surface may have a contour that substantially corresponds to a spherical portion of a generally spherical segment or has an elongated, partially oval shape, and may be configured to increase contact area with the articulating surface of the femur, reduce stress concentrations, and increase resistance to dislocation subluxation.

Abstract: A biometric sensor array system may include a skin contact layer, a flexible printed circuit board (“PCB”), and a plurality of force sensing resistors (“FSRs”). The flexible PCB may be positioned adjacent the skin contact layer and may have a connector tail. Each FSR may be positioned on the flexible PCB. The connector tail may be adapted to electrically connect the plurality of FSRs to a signal receiving component. The flexible PCB may be configured so that one or more of the plurality of FSRs may be trimmed away from the flexible PCB so that the connector tail is still adapted to electrically connect a remaining one or more of the plurality of FSRs to the signal receiving component.

Abstract: A tibial trial insert includes an upper plate and lower plate. An adjustment arrangement between the upper and lower plates is actuatable to adjust a gap between the upper and lower plates. The adjustment arrangement includes a first lift with a first lever arm arrangement and a second lift with a second lever arm arrangement. Each lever arm arrangement is indirectly connected to the upper and lower plates and pivotally movable to vary its length and adjust the gap between the upper and lower plates. The first lift includes an actuator coupled to the first lever arm arrangement. Actuation of the actuator varies the length of the first lever arm arrangement. The adjustment arrangement includes a coupling that couples the second lift to the first lift and configured such that the length of the second lever arm arrangement is varied synchronously to the first lever arm arrangement.

Abstract: A line of joint implant systems includes an implant including a cup to be affixed in one of the elements of the considered joint, defining a smooth inner cavity of substantially hemispherical shape. The implant also includes an insert, mobile within the inner cavity of the fixation cup and having its smooth outer surface intended to cooperate by ball-and-socket joint with the inner cavity, and defining in turn a smooth inner cavity of substantially hemispherical shape. The implant further includes a head or ball, solid with a second element of the joint, of spherical shape, intended to be received in the inner cavity of the mobile insert and to form a second ball-and-socket joint. The ratio of the inner diameter of the inner cavity of the fixation cup to the inner diameter of the inner cavity of the mobile insert is constant, whatever the diameter of the selected ball.

Abstract: An ankle implant for use in ankle arthroplasty in total ankle replacement is provided. The implant includes an upper prosthesis anchored to the tibia and a lower prosthesis anchored to the talus. The lower prosthesis is operable associated with the upper prosthesis. The implant also includes a stem which is rigidly removably connected to the second member. The stem includes a portion for attachment to the calcaneous. The stem is be adapted to be in a first position in the calcaneous when the stem is in a first relative position with respect to the lower prosthesis, and to provide for a second position in the calcaneous when the stem is in a second relative position with respect to the lower prosthesis.

Abstract: An orthopaedic prosthetic system includes a plate having one or more flanges and an acetabular shell component. Each flange includes a surface configured to engage a patient's bone. The plate also includes a central ring that engages a lip extending from an outer surface of the shell component. The ring may be mechanically attached to the lip using multiple fasteners. The system may include multiple plates each having a different configuration from other plates, and may also include multiple shell components each having a different configuration from other shell components. Methods for assembling and using the prosthetic system are also disclosed.

Abstract: The present invention provides an active substance application insert (10, 110) for an implant (30), in particular a joint implant. The active substance application insert has a main body (11), an active substance chamber (12) formed in the main body, an application side (13, 113) which forms a front face of the active substance chamber, wherein the application side has a plurality of application openings (14, 114), and a securing means (15) with which the main body can be detachably secured in the implant. In a state in which the main body is inserted into the implant, the application side faces outwards relative to the implant, such that the application openings connect the active substance chamber to the environment of the implant. Furthermore, within the scope of the present invention an implant (30) with a recess (31) for receiving an active substance application insert (10, 110) is provided.

Abstract: The invention relates to biomimetic, biodegradable composites including a magnesium (Mg) alloy mesh and a polymer/extracellular matrix (ECM). These hybrid composites, more particularly, are useful for the fabrication of medical implant devices, e.g., scaffolds, and are effective for bone regeneration. The fabrication process includes creating the Mg alloy mesh, and concurrently electrospinning the polymer and electrospraying the ECM onto the mesh.