Disclosed is a method for forming an orthopaedic implant. The method comprises determining one or more parameters of a bone, of a subject, to which the implant is to be attached, and calculating specifications based on parameters. That calculation includes calculating a mechanical property relating to elasticity of the implant, a length of the implant, and positions of two or more fixation locations by which to fix the implant to the bone. The method further comprises forming the implant based on the specifications, wherein each fixation location comprises a longitudinal axis through the implant, and calculating specifications comprises calculating a trajectory for the longitudinal axis of the respective fixation location.

Glenoid components with asymmetric fixation points are provided. Also, methods and devices are provided for the optimization of shoulder arthroplasty component design through the use of medical imaging data, such as computed tomography scan data. The methodology may improve the understanding of glenoid anatomy through the use of medical imaging data and 3D modeling, and for glenoid components that exploit this methodology. The methodology provides for how anatomical features change based on the specific location in the glenoid. The methodology can optimize loading and fit at the bone-device interface. Asymmetrical glenoid components are provided with significantly improved initial fixation.

A computer-generated component file for fabricating an orthopedic implant is prepared. First and second select sections of an initial implant model of a computer-aided design model are set to first and second model porous sections. A remaining section of the initial implant model is left. All regions defining the first and the second select sections are spaced not more than a preset distance from a patient-specific bone model of the computer-aided design model as measured uniformly. The first and the second model porous sections are merged with a remaining section of the initial implant model to form at least a portion of a final implant model. The final implant model is stored in a component file configured to be accessed by a computer-aided manufacturing machine for use in fabricating the orthopedic implant. At least a portion of the orthopedic implant corresponds to the final implant model.

An acetabular shell component includes a solid substrate, a porous outer layer coupled to the solid substrate, a porous inner layer coupled to the solid substrate, and an inner bearing coupled to the porous inner layer. One or more adjuncts extend outward from the porous outer layer. Each adjunct includes an outer surface that defines a customized patient-specific negative contour shaped to conform to a positive contour of a patient's bone. A method for manufacturing the acetabular shell component using an additive manufacturing process is also disclosed.

Implants for prevention of cold welding, corrosion and tissue overgrowth on surfaces between medical implant components include a first medical implant component having a first implant contact surface, a second medical implant component having a second implant contact surface positionally interfacing with the first implant contact surface of the first medical implant and a separation coating material on at least one of the first implant contact surface and the second implant contact surface. Methods for prevention of cold welding and/or corrosion between and/or tissue/bone overgrowth on implant components and methods of sealing an interface between a first implant component and a second implant component in a prosthesis system are also disclosed.

For a membrane encapsulated joint implant sealed under vacuum, a joint implant includes an outer cup, an inner cup, a joint head, a joint membrane, a lubricant, and an implant stem. The outer cup attached at a proximal bone. The nests within the outer cup and receives a joint head, the inner cup comprising an inner cup rim. The joint head is disposed within the inner cup and forms a bearing that rotates within the inner cup. The joint membrane sealed to the inner cup rim and vacuum seals the joint head within the inner cup to form a capsular space. The lubricant is disposed within the capsular space. The implant stem that is attached to a distal bone and that attaches through the joint head through the joint membrane.

A joint replacement device is provided that includes an inner surface configured to accommodate at least one of a portion of an outer surface of a femoral head of a femur and a prosthetic secured to the femoral head, an outer surface configured to accommodate at least one of a portion of an outer surface of an acetabulum socket and a prosthetic secured to a pelvis, wherein the inner surface and outer surface each have a circular curvilinear shape and together include an inner perimeter and an outer perimeter, and wherein the inner perimeter is joined to the outer perimeter to form a posterior limb and an anterior limb, and further including, a posterior portion, an anterior portion, and a superior portion formed from the inner surface and the outer surface; wherein the superior portion further includes a posterior superior portion and an anterior superior portion.

An acetabular cage or device (100) is disclosed. In one embodiment, the acetabular cage includes a cup portion (110) configured for implantation in an acetabulum and a flange (120) extending from the cup portion. The flange including a first, bone contacting surface (126) configured to face bony tissue surrounding the acetabulum when the cup portion is implanted into the acetabulum and a second, top surface (127) opposite the first surface. The flange includes a flexible portion (130) and a fixation portion (122), the fixation portion including one or more fixation features (124) configured to facilitate fixation of the flange to the bony tissue surrounding the acetabulum. The flexible portion is arranged and configured to enable the flange, and hence the fixation portion, to move relative to the cup portion to facilitate placement of the flange relative to the bony tissue.

A system for facilitating arthroplasty procedures includes a robotic device, a reaming tool configured to interface with the robotic device, and a processing circuit communicable with the robotic device. The processing circuit is configured to obtain a surgical plan comprising a first planned position of an implant cup and a second planned position of an implant augment relative to a bone of a patient, determine a planned bone modification configured to prepare the bone to receive the implant cup in the first planned position and the implant augment in the second planned position, generate one or more virtual objects based on the planned bone modification, control the robotic device to constrain the cutting tool with the one or more virtual objects while the cutting tool interfaces with the robotic device and is operated to modify the bone in accordance with the planned bone modification.

Prostheses, acetabular apparatuses, and methods of use are disclosed. In some embodiments, an acetabular apparatus includes an acetabular cup and an acetabular cage disposed within an interior of the acetabular cup. The acetabular cage may include a central portion including a first section and a second section rotatably coupled together, and a first flange extending from the first section and a second flange extending from the second section. The acetabular prosthesis may further include a fastener extending through each of the acetabular cup and the central portion of the acetabular cage.