Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 46585 - prosthesis, knee, internal, insert component - the pfc sigma tc3 fixed bearing inserts are made from uhmwpe and reinforced with titanium pins. the pin is part of the spine and protrudes down through the bottom of the insert. it is inserted into the hole of the modular tibial tray. the pfc sigma tc3 fixed bearing insert locks into the tibial tray and articulates with the femoral component. p.f.c sigma tc3 tibial fixed bearing inserts are offered in the same sizes as the femoral components with dimensions that correspond to the tibial tray. the pfc sigma tc3 fixed bearing insert is the articulating component of a total knee arthroplasty and for revision of failed knee prostheses. it is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheu

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 32832 - uncoated knee tibia prosthesis, metallic - the pfc sigma keel tibial tray is designed to replace the tibial condyles during bicondylar replacement of the knee joint and is made of titanium. the device is designed to hold the insert which articulates with the femoral prosthetic component of the knee joint. it is non-porous and its implantation is intended to be performed with bone cement. the pfc sigma keel tibial tray is the tibial component which holds the insert component of a total knee arthroplasty. it is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 33745 - coated knee femur prosthesis - the pfc sigma cruciate retaining porous femur is a primary bicondylar replacement prosthesis made of metal cobalt chrome. it articulates with the tibial insert of a knee joint prosthesis. it is coated with porocoat intended to improve fixation and stability by promoting bone ingrowth. the pfc sigma cruciate retaining (cr) porous femur are bicondylar femoral components which articulate with the insert component of a total knee arthroplasty and is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 32831 - uncoated knee femur prosthesis - the pfc sigma cruciate retaining non-porous femur are a primary bicondylar replacement prosthesis made of cobalt chrome. it is uncoated and its implantation is performed with bone cement. it articulates with the tibial insert of a knee joint prosthesis. the pfc sigma cruciate retaining (c/r) non-porous femurs are bicondylar femoral components which articulate with the insert component of a total knee arthroplasty and is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 46585 - prosthesis, knee, internal, insert component - the pfc sigma stabilised xlk fixed bearing insert articulates with the femoral implant and snap locks into the tibial tray of a knee joint prosthesis. it is a one-piece contoured polyethylene (pe) insert. the pfc sigma stabilised xlk fixed bearing insert is the articulating component of a total knee arthroplasty and is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 46585 - prosthesis, knee, internal, insert component - the pfc sigma curved rp insert articulates with the femoral component and rotates on the surface of the tibial tray of a knee joint prosthesis. it is a one-piece contoured uhmwpe insert. the pfc sigma curved rp insert is the articulating component of a total knee arthroplasty and is intended to replace the damaged knee joint articulation in patients with osteoarthritis and rheumatoid arthritis. indicated for use in skeletally mature individuals undergoing primary surgery for reconstructing knees damaged as a result of noninflammatory degenerative joint disease (nidjd) or either of its composite diagnoses of osteoarthritis and post-traumatic arthritis pathologies and for revision of failed knee prostheses.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 46585 - prosthesis, knee, internal, insert component - the pfc sigma duofix insert articulates with the femoral component and snap locks into the tibial tray of a knee joint prosthesis. it is a one-piece contoured polyethylene insert. the pfc sigma duofix insert is the articulating component of a total knee arthroplasty and is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 34198 - coated knee tibia prosthesis - the pfc sigma mbt porous tibial tray is designed to replace the tibial condyles during bicondylar replacement of the knee joint and is made of cobalt chrome. the device is designed to hold the mobile bearing insert which articulates with the femoral prosthetic component of the knee joint. it is porous coated and intended for cementless applications. the pfc sigma mbt porous tibial tray is the tibial resurfacing component which holds the mobile bearing insert component of a total knee arthroplasty. it is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 32832 - uncoated knee tibia prosthesis, metallic - the pfc sigma mbt cemented tibial tray is designed to replace the tibial condyles during bicondylar replacement of the knee joint; it is made of metal cobalt chrome. the device is designed to hold the mobile bearing insert which articulates with the femoral prosthetic component of the knee joint and its implantation is intended to be performed with bone cement. the pfc sigma mbt cemented tibial tray is the tibial resurfacing component which holds the mobile bearing insert component of a total knee arthroplasty. it is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.

Australia - English - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd t/a depuy synthes - 32832 - uncoated knee tibia prosthesis, metallic - the pfc mbt cemented keel tibial tray is designed to replace the tibial condyles during bicondylar replacement of the knee joint; it is made of metal cobalt chrome. the device is designed to hold the mobile bearing insert which articulates with the femoral prosthetic component of the knee joint and its implantation is intended to be performed with bone cement. the pfc sigma mbt cemented keel tibial tray is the tibial resurfacing component which holds the mobile bearing insert component of a total knee arthroplasty. it is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. candidates for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or failed previous implant.