Abstract: An ankle arthroplasty system may have a talar prosthesis and a tibial prosthesis, each of which has an articular surface and a bone engagement surface. Each bone engagement surface may have an anterior-posterior curvature and a medial-lateral curvature with a convex shape. A burr with a rotatable cutting element may be used to form a prepared surface on the talus or the tibia to receive the corresponding prosthesis. A cutting guide may be used to guide motion of the burr; the cutting guide may include a base and an arm movably coupled to the base. One of the base and the arm may have a guide surface, and the other may have a follower that slides along the guide surface to constrain motion of the burr such that the prepared surface has at least one concave curvature and one convex curvature.

Abstract: An ankle arthroplasty system may have a talar prosthesis and a tibial prosthesis, each of which has an articular surface and a bone engagement surface. Each bone engagement surface may have an anterior-posterior curvature and a medial-lateral curvature with a convex shape. A burr with a rotatable cutting element may be used to form a prepared surface on the talus or the tibia to receive the corresponding prosthesis. A cutting guide may be used to guide motion of the burr; the cutting guide may include a base and an arm movably coupled to the base. One of the base and the arm may have a guide surface, and the other may have a follower that slides along the guide surface to constrain motion of the burr such that the prepared surface has at least one concave curvature and one convex curvature.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Devices and methods are disclosed for joint replacement.

Abstract: Joint replacement spacers that fully seat against the cut surface of a bone while remaining free to move on the cut surface within prescribed limits; methods of joint replacement using such spacers.

Abstract: An implant for metatarsal hemiarthroplasty according to embodiments of the present invention includes a resurfacing body configured to at least partially resurface distal and dorsal surfaces of an articular head of a metatarsus, the resurfacing body including a first side and a second side, the first side configured to articulate against a phalange associated with the metatarsus, the first side including a convex surface formed of ceramic, the second side configured to be fixed to the metatarsus, the second side including a concave surface from which protrude at least two immobilization elements, the at least two immobilization elements configured to interface with the articular head.

Abstract: Methods of implanting an ankle prosthesis in a subject having an ankle joint in need of replacement.

Abstract: Methods of implanting an ankle prosthesis in a subject having an ankle joint in need of replacement.

Abstract: A fixed-bearing ankle prosthesis may include tibial and talar components whose articulating surfaces directly contact one another. The tibial component defines medial and lateral concave condylar facets separated by a convex central portion. The talar component includes medial and lateral convex condyles separated by a concave central portion. The condyles each have a single radius of curvature in a medial-lateral plane such that each condyle has a circular-arc cross-section continuously extending from the respective medial or lateral edge of the talar component to the concave central portion. The medial-lateral radii of the condyles are smaller than corresponding radii of the condylar facets.

Abstract: The present invention is directed to prosthetic knee joints having femoral and tibial components. More particularly, in one embodiment the knee joint prosthesis of the present invention includes an auxiliary pair of load bearing surfaces in addition to other load bearing surfaces of the tibial and femoral components, which are the medial tibial and femoral condyles, the lateral tibial and femoral condyles, and the central tibial and femoral cam surfaces. The auxiliary pair of load bearing surfaces are located on the tibial component, posterior (i.e, on the rear side of the knee joint) to the central cam, centered between the tibial condyles, and on the femoral component, posterior to the femoral central camming surface, centered between the femoral condyles.

Abstract: An instrument is provided for use in shaping a femur preparatory to implantation of a knee prosthesis. A gap checking device is fixed to the distal end of the patient's femur and referenced to the epicondyles of the femur. The gap checking device includes slots through which a cutting instrument can be passed to shape the femur so that it can receive the femoral component of the prosthesis. One of the slots enables the distal femoral cut to be made. The thickness of the gap checking device is selected so that the distance between the distal femoral cut and the distal surface of the gap checking device plus the thickness of a shim resting on the cut proximal tibia surface is equal to the combined thickness of the tibial and femoral components of the prosthesis. This enables balancing of the ligaments to be checked before the femoral cuts are made, but while the gap checking device is secured to the femur.

Abstract: The present invention is directed to prosthetic knee joints having femoral and tibial components.

Abstract: Disclosed is a method of producing a shaped article suitable for use as the load bearing component of a prosthetic device formed from ultrahigh molecular weight polyethylene. polyethylene.

Abstract: A method for preserving a component including polymeric material that reduces oxidation degradation after irradiation. The method includes sealing the polymeric material in a container filled with a fluid, preferably a liquid. Monitoring the integrity of the container's seal is enhanced by use of liquid rather than a gas. The method can be used for long term storage of orthopaedic implants which include polymeric material, especially Ultra High Molecular Weight Polyethylene.