The present invention provides a uni-compartmental knee joint prosthesis (1) which includes a tibial component (2) and a femoral component (3). The tibial component (2) has a fixation portion (10) adapted to be fixed to an upper end of a prepared tibia (T) in a patient, and a bearing portion (30) presenting an articulation surface (32) formed from a ceramic material, wherein the bearing portion (30) is adapted for movement relative to the fixation portion (10). The femoral component (3) is adapted to be fixed to a lower end of a prepared femur (F) in a patient, and comprises a body portion (50) presenting an articulation surface (56) formed from a ceramic material for engagement with the articulation surface (32) of the tibial component (2). The articulation surfaces (32, 56) of the tibial and femoral components are adapted for essentially congruent engagement over a full range of movement of the prosthesis.

The fusion device for fusing a synovial joint of a human or animal patient, in particular a human facet joint, finger joint or toe joint, includes two pin-shaped anchorage portions and arranged therebetween a stabilization portion. The anchorage portions include a thermoplastic material which is liquefiable by mechanical vibration. The stabilization portion preferably has a surface which is equipped for enhancing osseointegration. The anchorage portions have a greater thickness and a greater depth than the stabilization portion. Then the fusion device is pushed between the articular surfaces and mechanical vibration, in particular ultrasonic vibration, is applied to the proximal face of the fusion device. Thereby the liquefiable material is liquefied where in contact with the bone tissue and penetrates into the bone tissue, where after re-solidification it constitutes a positive fit connection between the fusion device and the bone tissue.

A fusion cage has a first component that defines an outside surface that is configured to engage a vertebral endplate, and an interior surface. The fusion cage has a second component that defines first and second opposed surfaces. One of the first and second opposed surfaces can mate with the interior surface of the first component. The fusion cage can include vertical and lateral throughholes adapted to enhance fusion.

A total knee prosthesis to be implanted in a human patient includes a femoral element having a longitudinal axis, a tibial plateau having a longitudinal axis and a mobile plate. The mobile plate is interposed between the femoral element and the tibial plateau to form two joints with them wherein: a) the surfaces of mutual friction of the femoral element with the mobile plate and the surfaces of mutual friction of the tibial plateau with the mobile plate are entirely constituted by one and the same massive ceramic material; and b) the mobile plate includes two condylar bowls, and the femoral element includes two condyles, the condyles and the condylar bowls each having surfaces of mutual friction spaced apart from each other by a distance smaller than 100 μm when the longitudinal axes of the femoral element and the tibial plateau form an angle of 0° to 75°.

The invention relates to a method and a device for producing an implant, wherein a natural bone microstructure of a natural bone region is detected (S1), an implant region in the natural bone region is marked (S2), the detected bone microstructure in the marked implant region is analysed to determine reproduction parameters (S3), and on the basis of the determined reproduction parameters, an artificial microstructure for producing the implant is created (S4).

Disclosed herein are methods for functionalizing the surface of a biomedical implant. The biomedical implant may be a zirconia-toughened alumina implant surface functionalized with silicon nitride powder for promoting osteogenesis.

The present disclosure relates generally to the field of mammalian prosthetics, and more specifically to prostheses for use in total or partial joint replacement, and to a method of use of these prostheses in arthroplasty. Thus, disclosed is a prosthesis for use in hip arthroplasty that comprises an artificial femoral head that includes a head portion constructed totally or partially of a polymeric material, and a connector means designed to connect said head portion in a non-articulating manner to a femoral stem portion. The head portion may be made solely of solid polymeric material or of an outer shell of polymeric material connected in a non-articulating manner to an embedded core. The polymeric material is preferably selected from ultra-high molecular weight polyethylene (UHMWPE) or radiation treated UHMWPE having substantially no detectable free radicals. The embedded core comprises, for example, one or more of solid non-polymeric material (e.g., metallic, ceramic, or ceramic-on-metal material), a multiplicity of metallic spokes, a metallic scaffolding, and/or combinations thereof.

A system for replacing a portion of an articular surface including providing an implant site and installing an implant into the implant site. The implant site includes a first and a second excision site which at least partially intersect with one another. Each of the first and second excision sites are formed by providing a respective axis and excising a portion of the articular surface relative to the respective axes.

A separate nub component between the plate and an intervertebral fusion cage, wherein the nub is attached to the plate. The nub lessens the undesired pivotal movement of the plate. It is believed that when the nub fits snugly between the endplates of the adjacent vertebral bodies, it acts as a stop against the undesired pivotal movement of the plate.

A zirconia material manufacturing method includes: dispersing hydroxyapatite powder in water to prepare a slurry having a hydroxyapatite powder concentration of 1%; and dipping zirconia in the slurry to form, on the zirconia, a coating layer containing hydroxyapatite.