Abstract:
Solid-state deformation processing of crosslinked high molecular weight polymers such as UHMWPE, for example by extrusion below the melt transition, produces materials with a combination of high tensile strength and high oxidative stability. The materials are especially suitable for use as bearing components in artificial hip and other implants. Treated bulk materials are anisotropic, with enhanced strength oriented along the axial direction. The material is oxidatively stable even after four weeks of accelerated aging in a pressure vessel containing five atmospheres of oxygen (ASTM F2003). Because of its oxidative stability, the deformation processed material is a suitable candidate for air-permeable packaging and gas sterilization, which has thus far been reserved for remelted crosslinked UHMWPE.
Abstract:
The present invention is directed to a modular shoulder prosthesis measuring device having an adjustable radial offset provided by relative rotation of an adapter interdisposed between the stem and the head. Specifically, the interface configuration between the stem and the adapter, as well as between the adapter and the head are designed such that relative positioning of these components provides a continuous adjustment in the radial offset. Indicia are provided to precisely determine the magnitude and direction of the adjustment being made.
Abstract:
A prosthetic system for replacement of a portion of a hip bone including a plurality of acetabular components and a plurality of flange components. The prosthetic system also includes a plurality of pubis components. Each of the pubis components and each of the flange components are operable to connect to each of the acetabular components. Each of the pubis components define a clamping portion that is configured to attach to an opposed healthy pubis bone. An angle between the flange component and the pubis component varies among the acetabular components.
Abstract:
Medical implants having a ceramic body reinforced with a plurality of metal wires. Methods of making the implant and methods of implanting the medical implant are also provided.
Abstract:
A ceramic implant having a rough surface texture and a method for forming the same. The method includes forming a green body of a first ceramic composition. The green body is reduced to smaller pieces thereby forming ceramic fragments. A mold is filled with a second ceramic composition to form a ceramic base. Ceramic fragments are added to the mold and an outer layer is formed over at least a portion of the ceramic base. Pressure is applied to the mold to compress the outer layer onto the ceramic base and to form a green assembly. The green assembly is sintered to form a ceramic implant having a rough surface texture.
Abstract:
A prosthesis for replacing a portion of the anatomy including an outer bone engaging surface and an inner bearing surface. The prosthesis may include a rim disposed between the inner bearing surface and the outer bone engaging surface. The rim may include at least one contour operable to reduce loading on the rim.
Abstract:
A bone augment for repairing a bone defect. The bone augment includes a porous body and a metallic liner. The porous body defines a bore and is configured to be intraoperatively shaped to correspond to the bone defect. The metallic liner is injection molded within the bore such that portions of the liner interlock with pores of the porous body. The metallic liner is operable to mount an implant to the bone augment.
Abstract:
A press-fit prosthesis for replacing a portion of a bone. The prosthesis can comprise a first side and a second side opposite the first side. The second side can be operable to engage the bone. The prosthesis can include at least one resorbable fixation member coupled to the second side such that the at least one resorbable fixation member does not extend through to the first side. The at least one resorbable fixation member can be coupled offset from a center of the second side. The at least one resorbable fixation member can substantially resist movement of the prosthesis relative to the bone. The at least one resorbable fixation member can resorb at a rate that enables bone in-growth to fixedly couple the prothesis to the bone.
Abstract:
A modular proximal interphalangeal joint implant assembly including a first stem component, a second stem component, and an articulation assembly. The first stem component includes a first locking device and is operable to be implanted in a proximal phalanx bone. The second stem component includes a second locking device and is operable to be implanted in a middle phalanx bone. The articulation assembly includes a first articulation component operable to be removably attached to the first locking device and a second articulation component operable to be removably attached to the second locking device. The articulation assembly can include a semi-constrained articulation assembly or a constrained articulation assembly.
Abstract:
An elbow prosthesis can include a capitellar implant that has an articulating head and a stem. The articulating head can have a first substantially hemispherical portion and a second portion that collectively extend between lateral and medial sides of the articulating head and are separated by a plane. The first and second portions can generally extend between the lateral and medial sides. The second portion can generally have an attachment lobe that extends on the lateral side and that defines a passage therethrough. The passage can extend at least partially on the second portion.