SIGMA PHARMACEUTICALS PTY LTD - search results

johnson & johnson medical pty ltd t/a depuy synthes - 33580 - uncoated knee tibia prosthesis, polyethylene - the pfc sigma posterior stabilised all poly insert replaces the tibial condyles during bicondylar replacement of the knee joint; it is made entirely of polyethylene. the device is designed to articulate directly with the femoral prosthetic component and its implantation is intended to be performed with bone cement. the pfc sigma posterior stabilised all poly insert is the tibial 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.

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

pfc sigma tc3 femur - uncoated knee femur prosthesis

johnson & johnson medical pty ltd t/a depuy synthes - 32831 - uncoated knee femur prosthesis - the pfc sigma tc3 femoral is manufactured from co-cr-mo alloy and is uncoated for cemented fixation. the femoral condylar component matches the tibial bearing component. the femoral components are available in right and left configurations. the pfc sigma tc3 femorals allow for the attachment of femoral augments, sleeves, and ancillary p.f.c. stem extensions to provide additional stability to accommodate for femoral bone loss. the pfc sigma tc3 femur is the femoral 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 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 a failed previous implant.

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

pfc sigma modular titanium tibial tray - uncoated knee tibia prosthesis, metallic

johnson & johnson medical pty ltd t/a depuy synthes - 32832 - uncoated knee tibia prosthesis, metallic - the pfc sigma modular titanium tibial tray replaces the tibial condyles during total knee replacement and articulates with the femoral implant. it is a fixed bearing tibial tray and made from titanium with uhmwpe distal stem plugs. fins support the plateau, resists rotational forces and anterior/posterior rocking of the tibial component. an insert containment rim enhances tray strength and captures the insert. it is non-porous and implantation is intended to be performed with bone cement. the pfc sigma modular titanium tibial tray is the tibial component of 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)

pfc sigma modular tibial tray - cocr - prosthesis, internal, joint, knee, tibial component - uncoated knee tibia prosthesis, met

johnson & johnson medical pty ltd t/a depuy synthes - 32832 - uncoated knee tibia prosthesis, metallic - the pfc sigma modular tibial tray - cocr is designed to replace the tibial condyles during bicondylar replacement of the knee joint and is made of cocr with a highly polished top surface. the i2 locking mechanism locks in the tibial insert which decreases micro-motion. implantation is intended to be performed with bone cement. the pfc sigma modular tibial tray - cocr is the tibial resurfacing 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.