A ceramic monobloc femoral component (10) is provided for a total hip replacement prosthesis. The ceramic monobloc femoral component (10) has a ceramic femoral stem (14) and a ceramic head (12) which defines a part-spherical articular surface receivable by an acetabular cup (56). The ceramic femoral stem (14) and the ceramic head (12) are integrally formed as one-piece.

A humeral implant component connectable to another humeral implant component, the humeral implant component comprising: a longitudinal axis, a first end and a second end, the first end and the second end opposing each other along the longitudinal axis of the humeral implant component, and an interface part for connecting the humeral implant component to the other humeral implant component, wherein the interface part is tapered along the longitudinal axis in a direction from the second end to the first end, the interface part being engageable with a tapered interface part of the other humeral implant component to form a tapered connection between the humeral implant component and the other humeral implant component, wherein the humeral implant component further comprises a through hole extending along the longitudinal axis for locking the tapered connection by a longitudinal fastener.

The disclosure relates to a replacement member for a shoulder joint replacement comprising an attachment face on one side of the member, a concave joint surface on a side of the replacement member opposite to the side of the attachment face, and a circumferential face connecting the attachment face and the joint surface. A portion of the concave joint surface is connected to at least a portion of the circumferential face via a chamfered or rounded edge.

A tibial implant includes one or more stiffness-modifying features to reduce the stiffness of one or more sections of the tibial implant. The stiffness-modifying features may include slots, recesses, or passageways defined in various locations of the tibial implant to selectively reduce the stiffness of a tibial insert and/or tibial base of the tibial implant.

The present disclosure relates to expandable interbodies that include superior and inferior shells and a control assembly positioned between and inside of the shells, the control assembly including nested cages operably connected to each other with an adjustment screw. Rotation of the adjustment screw translates the cages relative to each other, which in turn causes the shells to open or expand.

A knee prosthesis (e.g., a tibial implant or component) is disclosed. In one embodiment, the tibial implant includes a load bearing component (e.g., a tibial tray) and a support member arranged and configured to be at least partially positioned within an intramedullary canal of a patient's bone. In some embodiments, the tibial implant may also include one or more pegs positioned anteriorly on a bottom surface of the tray and one or more bridges for coupling the pegs to the support member so that loads received by the pegs are transferred to the support member via the bridge. In addition, and/or alternatively, the tibial implant may include one or more chamfers or loading zones for elongating the transition area between the support member and the bottom surface of the tibial tray to extend the area over which the load is transferred.

A method of repairing a fractured humerus may include implanting a prosthetic humeral stem into a humeral canal of the fractured humerus. First and second tuberosities of the fractured humerus may be robotically machined to include first and second implant-facing surfaces that are substantially negatives of first and second surface portions of the proximal end of the prosthetic humeral stem. The first and second tuberosities may be machined so that the first and second tuberosities have first and second interlocking surfaces shaped to interlock with each other. During implantation, the first and second implant-facing surfaces are in contact with the first and second surface portions of the proximal end of the prosthetic humeral stem, and the first interlocking surface interlocks with the second interlocking surface.

The invention relates to a fastening device for an implant that is elastically deformable by stress, the length of the device in the unstressed state being less than that of the device in the stressed state, and the diameter of the device in the unstressed state being greater than that of the device in the stressed state, and to a kit comprising it.

An implantable medical device is disclosed comprising a thermoplastic composite body having anterior, first lateral, second lateral, posterior, superior, and inferior surfaces, and at least one dense portion and at least one porous portion which are integrally formed. The at least one dense portion is formed of a first thermoplastic polymer matrix that is essentially non-porous, and which is continuous through a thickness dimension from the superior surface to the inferior surface. The at least one porous portion is formed of a porous thermoplastic polymer scaffold having a second thermoplastic polymer matrix which is continuous through the thickness dimension. A method for forming the thermoplastic composite body is disclosed comprising disposing a first powder mixture in a first portion of a mold, disposing a second powder mixture in a second portion of the mold, simultaneously molding the first powder mixture and the second powder mixture, and leaching porogen.

The invention features a glenoid (shoulder socket) implant prosthesis, a humeral implant prosthesis, devices for implanting glenoid and humeral implant prostheses, and less invasive methods of their use for the treatment of an injured or damaged shoulder.