An implant includes a body including a substrate and a bone interfacing lattice disposed on the substrate. The bone interfacing lattice includes at least two layers of elongate curved structural members. In addition, the at least two layers of elongate curved structural members include a first layer adjacent the substrate and a second layer adjacent the first layer. Also, the first layer has a first deformability and the second layer has a second deformability, wherein the second deformability is greater than the first deformability.

A femoral component (2) for mounting onto a femur and being adapted to articulate with a tibial bearing component in a knee prosthesis comprises proximal end portions (7, 10) adapted to be oriented towards the femur when the femoral component (2) is mounted thereon, and distal end portions adapted to be oriented towards the tibial bearing component when the knee prosthesis is fully extended. The proximal end portions (7) comprise posterior proximal end portions which are located on an posterior side of the femoral component and an anterior proximal end portion (10) which is located on an anterior side of the femoral component (2). The femoral component (2) further comprises a medial condyle (13) and a lateral condyle (14) which each extend from one of the posterior proximal end portions beyond the distal portions and towards the anterior proximal end portion (10) of the femoral component (2). The medial and lateral condyles (13, 14) form a condylar gap between each other, wherein the medial condyle (13) and the lateral condyle (14) are shaped to articulate with the tibial bearing component through a range of motion, in which a full extension of the knee prosthesis corresponds to zero degrees flexion of the knee prosthesis and positive flexion corresponds to greater than zero degrees flexion of the knee prosthesis. The femoral component (2) further comprises a sagittal plane extending in a proximal/distal direction and further extending through the condylar gap from the anterior side to the posterior side of the femoral component (2). A patellar groove (16) extends from the condylar gap towards the anterior proximal end portion (10) of the femoral component (2) along a mathematical curve (17). The mathematical curve (17), when looking onto the anterior side of the femoral component, is canted towards a medial side (18) of the femoral component (2) relative to the sagittal plane when the patellar groove (16) extends proximally.

The patellar groove (16) is formed by a concave groove section (19) on the anterior side of the femoral component (2), the groove section (19) having a groove base (20). The femoral component (2) further comprises a medial ridge section (21) and a lateral ridge section (22) which are disposed adjacent the groove section (19) and each have a convex shape. The medial ridge section (21) forms the medial condyle (13) and a medial extension (23) to the medial condyle (13) towards

Disclosed herein are implants with pivots that can be rotated about these pivots to be implanted onto bone, and methods for implanting same. The implant may have a plurality of pivot pads and curved projections extending from one or more bone contacting surfaces. The pivot pads and curved projections may engage with corresponding features on bone for implantation and securement of the implant to the bone. The implant may be rotated about the plurality of pivot pads placed in corresponding recesses on bone to seat the projections into the corresponding recesses.

The present disclosure discloses an artificial femoral prosthesis (100) for knee arthroplasty, a tibial prosthesis (150), a medial femoral unicompartmental prosthesis (201), a lateral femoral unicompartmental prosthesis (301), and a femoral trochlear prosthesis (401). The femoral prosthesis (100) comprises: a medial condyle portion (51) and a medial trochlear portion (131), wherein an articular surface of the medial condyle portion appears in a sagittal section as an arc of a first ellipse (38), and an articular surface of the medial trochlear portion appears in the sagittal section as an arc of a second ellipse or circle (40); and lateral members (91, 141), comprising a lateral trochlear portion (141) and a lateral condyle portion (91), wherein an articular surface of the lateral trochlear portion appears in the sagittal section as an arc of a third ellipse or circle (80), and an articular surface of the lateral condyle portion appears in the sagittal section as an arc of a fourth ellipse (78). The prostheses according to the above embodiments of the present disclosure can better conform to geometric shapes of normal femoral condyles of humans, thereby simplifying greatly design of parameter values for different models of femoral prostheses.

Hard-tissue implants are provided that include a bulk implant, a face, pillars, slots, and at least one support member. The pillars are for contacting a hard tissue. The slots are to be occupied by the hard tissue. The at least one support member is for contacting the hard tissue. The hard-tissue implant has a Young's modulus of elasticity of at least 3 GPa, and has a ratio of the sum of (i) the volumes of the slots to (ii) the sum of the volumes of the pillars and the volumes of the slots of 0.40:1 to 0.90:1. Methods of making and using hard-tissue implants are also provided.

An orthopaedic prosthesis includes a femoral component comprising polymeric materials. The polymeric materials may include a polyaromatic ether or a polyacetal. The orthopaedic prosthesis may include a component having an articular layer and a support layer adjacent the articular layer. The support layer may include a reinforcement fiber. The orthopaedic prosthesis may be a knee prosthesis.

An implant has a soft tissue attachment structure, and a surface defining a trough. An ingrowth plate spans a portion of the trough and defines a suture tunnel between the ingrowth plate and the trough for receiving suture. The ingrowth plate bows convexly away from the surface and is perforated to facilitate long-term ingrowth and biologic fixation of soft tissue to the implant.

A combined fully organic high molecular material artificial knee joint, comprising a femur condyle (2), a tibia holder (4) and a tibia liner (3), the femur condyle (2) and the tibia holder (4) being formed by polyether ether ketone (PEEK) or derivatives thereof, and the tibia liner (3) being formed by ultra-high molecular weight polyethylene (UHMWPE). The tibia holder (4) comprises a platform (6) and a stable wing positioning portion (5) vertical thereto; upper and lower ends of the tibia liner (3) are jointed with the femur condyle (2) and the platform (6) respectively; the femur condyle (2) buffers a slide surface of the tibia liner (3); and the tibia holder (4) can finely move relative to a fixed surface of the tibia liner (3), and buffering of the femur condyle (2) against the slide surface of the tibia liner (3) matches fine movement of the tibia holder (4) relative to the tibia liner (3). Main parts of all implant components of the artificial knee joint are formed by high molecular materials, thereby relieving allergy and toxicity problems probably caused by metal and metal corrosion; PEEK elastic modulus matches a natural bone, thereby relieving a stress shield problem; a wearing problem is greatly relieved by means of the combination of buffering of the PEEK femur condyle (2) against the slide surface of the UHMWPE tibia liner (3) and fine movement of the tibia holder (4) relative to the fixed surface of the UHMWPE tibia liner (3); and meanwhile, by adding enhancement and developing components, the practicality is further improved.

An orthopaedic prosthesis system and associated instrumentation is disclosed. The system includes femoral and tibial components configured to be used in a number of different implanted configurations. The instrumentation is configured to facilitate preparation of the bones and selection of the implant configuration. A method of using the system is also disclosed.

An orthopaedic prosthesis system and associated instrumentation is disclosed. The system includes femoral and tibial components configured to be used in a number of different implanted configurations. The instrumentation is configured to facilitate preparation of the bones and selection of the implant configuration. A method of using the system is also disclosed.