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

zimmer biomet pty ltd - 34198 - coated knee tibia prosthesis - porous titanium alloy and ha coated cobalt chrome alloy tibial component with finned stem for enhanced rotational stability, and highly polished surface finish. designed for use as a component of a rotating platform total knee prosthesis, and may be used with modular stem options. trays grow medic-laterally in 4mm increments. porous titanium and hydroxyapetite coated cobalt chrome alloy tibial component of the vanguard rocc rotating platform total knee prosthesis. indications for use: osteoarthritis, rheumatoid arthritis and bone necrosis affecting two knee compartments; correction of genu varus, genu valgus or post-traumatic deformities; sequelae of prior procedures. the porous ha coating is intended for cementless fixation

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

zimmer biomet pty ltd - 32831 - uncoated knee femur prosthesis - cobalt chrome alloy femoral knee component intended for cemented fixation. the deep trochlear groove provides support for the patella in deep flexion and aids the quadriceps tendon. the posterior condyles grow proportionally in size, providing increased bone coverage, aiding high flexion and restoring femoral offset. the broad posterior condyles provide a large contact area in deep flexion dissipating forces more effectively. cobalt chrome alloy femoral component of the vanguard rocc rotating platform total knee prosthesis. indications for use: osteoarthritis, rheumatoid arthritis and bone necrosis affecting two knee compartments; correction of genu varus, genu valgus or post-traumatic deformities; sequelae of prior procedures. the device is intended for cemented fixation.

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

zimmer biomet pty ltd - 34199 - polyethylene patella prosthesis - arcom direct compression moulded polyethylene patella implant for cemented fixation; 3 peg, 1o mm thickness. designed for use as a component of a rotating platform knee prosthesis. arcom uhmwpe patella component of the vanguard rocc rotating platform total knee prosthesis. indications for use: osteoarthritis, rheumatoid arthritis and bone necrosis affecting two knee compartments; correction of genu varus, genu valgus or post-traumatic deformities; sequelae of prior procedures. the full pe patella is intended for cemented fixation.

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

zimmer biomet pty ltd - 33665 - posterior-stabilized total knee prosthesis - the vanguard ssk dcm constrained standard post tibial bearing is constructed of direct compression moulded arcom uhmwpe and articulates with the femoral and tibial tray components of the vanguard super stabilized knee system. the device has a swept back tibial post and deep anterior cutout. the constrained bearing allows +/- 1mm varus/valgus lift-off and +/- 0.5mm rotational freedom. the vanguard ssk direct compression moulded arcom uhmwpe constrained standard post tibial bearing is intended for use in revision cases with limited bone loss on the femoral side, as part of the vanguard ssk revision system. indications for use include: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or posttraumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

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

zimmer biomet pty ltd - 33745 - coated knee femur prosthesis - porous and ha coated cobalt chrome alloy femoral component designed with narrow anterior flange medio-laterally and deep trochlear groove, with proportional posterior condyles. the device is a rotating platform knee prosthesis with cementless fixation. porous titanium and hydroxyapetite coated cobalt chrome alloy femoral component of the vanguard rocc rotating platform total knee prosthesis. indications for use: osteoarthritis, rheumatoid arthritis and bone necrosis affecting two knee compartments; correction of genu varus, genu valgus or post-traumatic deformities; sequelae of prior procedures. the device is intended for cementless fixation.

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

zimmer biomet pty ltd - 33665 - posterior-stabilized total knee prosthesis - tibial bearing constructed of direct compression moulded arcom uhmwpe. the device has a deep anterior cutout; curved tibial post; provides high dislocation height; increased post/box contact at 90 deg flexion; allows for varus/valgus lift-off and 15 degrees internal/external rotational freedom. the vanguard ssk direct compression moulded arcom uhmwpe non?constrained posterior stabilised standard post tibial bearing is intended for use as one component of the vanguard super stabilised knee system. indicated for revision and complex primary indications where high degree of valgus/varus support is required and femoral bone loss is limited. mcl does not have to be intact but must provide some stability; replaces acl, pcl, lcl. indications for use: painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved; correction of varus, valgus, or posttraumatic deformity; correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

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

zimmer biomet pty ltd - 34198 - coated knee tibia prosthesis - titanium porous and ha coated cobalt chrome and titanium alloy tibial component with finned stem and highly polished tray to reduce coefficient of friction with tibial bearing. designed for use as a component of a rotating platform total knee prosthesis. nine tibial tray sizes with proportional stems. ha porous coating intended for cementless application' coating intended for cementless application porous titanium and hydroxyapetite coated cobalt chrome alloy tibial component of the vanguard rotating platform total knee prosthesis. indications for use: osteoarthritis, rheumatoid arthritis and bone necrosis affecting two knee compartments; correction of genu varus, genu valgus or post-traumatic deformities; sequelae of prior procedures. the porous ha coating is intended for cementless fixation

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - the tibial bearing is constructed of direct compression moulded arcom uhmwpe and articulates with the femoral and tibial tray components in patients requiring posterior cruciate substitution. the vanguard posterior stabilised uhmwpe tibial bearing is designed for use in treatment of low demand, less active or sedentary patients requiring posterior cruciate substitution, as one component of the vanguard total knee system. the indications for use: 1. painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. 2. correction of varus, valgus or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - the tibial bearing is constructed of direct compression moulded arcom uhmwpe and articulates with the femoral and tibial tray components in patients with intact posterior cruciate ligaments. standard or lipped shape options are provided for intra-operative flexibility to meet patient needs and surgeon preference. the vanguard cruciate retaining uhmwpe tibial bearing is designed for use in treatment of low demand, less active or sedentary patients, with intact cruciate ligament, as one component of the vanguard total knee system. the indications for use: 1. painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. 2. correction of varus, valgus or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

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

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - the tibial bearing is constructed of e1 antioxidant infused direct compression moulded uhmwpe and articulates with the femoral and tibial tray components in patients with intact posterior cruciate ligaments. the bearing provides for 15 degrees internal/external rotation, no varus/valgus constraint and includes a 3 degree posterior slope the vanguard e1 cruciate retaining uhmwpe tibial bearing is intended for use in conjunction with biomet tibial trays in both primary and revision applications, with or without bone cement, in patients with intact cruciate ligaments. the indications for use: 1. painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis and/or traumatic arthritis, where one or more compartments are involved. 2. correction of varus, valgus or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.