أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - tibial component of the nexgen rotating hinge knee prosthesis system intended for flexion/extension and internal/external rotation between the femoral and tibial components, but is constrained in the anterior/posterior and medial/lateral directions by means of a femoral hinge post extension. tibial components are made from zimaloy® cobalt-chromium-molybdenum alloy and are for non-modular cemented use only. intended to repair or replace the tibial knee joint, for patients with mderate to severe knee instability, significant bone loss and/or ligament deficiencies caused by neoplasms, trauma, rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders, and/or avascular necrosis of the femoral condyle, valgus, varus, or flexion deformities, the salvage of previously failed surgical attempts.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - tibial component of a coupled total knee replacement. constructed from cocrmo alloy with titanium nitride coating to prevent allergic reactions. m-o-m components are coupled by the metal-on-metal connecting mechanism. it is recommended to use the m-o-m components in case of an extra-articular resection.connects to various tibial stems & spacers as part of a modular universal tumour and revision system (mutars). a component of the mutars system intended to replace the tibial articulating surfaces of the knee. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

life healthcare pty ltd - 34198 - coated knee tibia prosthesis - tibial component of a coupled total knee replacement. constructed from cocrmo alloy with titanium nitride coating to prevent allergic reactions. m-o-m components are coupled by the metal-on-metal connecting mechanism. it is recommended to use the m-o-m components in case of an extra-articular resection. connects to various tibial stems & spacers as part of a modular universal tumor and revision system (mutars). a component of the mutars system intended to replace the tibial articulating surfaces of the knee. primary indication for the use of the mutars systems is after bone resection because of a tumour. further indications for the use of the mutars systems are massive bone loss such as in morbus gorham or for the revision arthroplasty and for the prosthetic treatment in case of fractures, pseudarthrosis and arthrosis

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

stryker australia pty ltd - 33692 - rotating hinged total knee prosthesis - tibial bearing component assembled intraoperatively with a set of bushings and an axle and a bumper.this assembly provides motion through the axle/bushing combination in the flexion/extension plane. the stem of the tibial bearing component fits into the polyethylene tibial component or insert which is fixed to the tibia, providing motion in the rotational plane and translation in the axial plane. made from vitallium alloy. a tibial bearing component of a modular rotating hinge knee system, intended to be implanted in the following condition(s): 1. there is destruction of the joint surfaces, with or without significant bone deformity. 2. the cruciate and/or collateral ligaments do not stabilize the knee joint. 3. the ligaments are inadequate and/or the musculature is weak. and/or, 4. revision is required of a failed prostheses where there has been gross instability, with or without bone loss or inadequate soft tissue

أستراليا - الإنجليزية - 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.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 33667 - trabeculated knee tibia/insert prosthesis - cruciate retaining (cr) tibial component designed for use with a functional cruciate ligament in conjunction with a cr or cra femoral component. cr tibias have a monoblock design where the polyethylene (uhmwpe) is directly molded into the tantalum (trabecular metal) base plate. the undersides of the monoblock tibias possess two hexagonal-shaped trabecular metal posts. it is available in multiple thickness options to facilitate soft tissue tensioning and joint line restoration. the nexgen? trabecular metal cr tibial component is intended for use where severe degeneration, trauma, or other pathology of the knee joint indicates cemented or cementless total knee arthroplasty.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 33667 - trabeculated knee tibia/insert prosthesis - posterior stabilized(lps) tibial component designed for use with both cruciate ligaments excised and in conjunction with a lps femoral component. it is manufactured from tantalum (trabecular metal) and ultra-high-molecular-weight-polyethylene(uhmwpe) and is available in multiple thickness options to facilitate soft tissue tensioning and joint line restoration. the device is pegged, and the undersides of the device possess two hexagonal-shaped trabecular metal posts. the nexgen® trabecular metal lps tibial components are intended for use where severe degeneration, trauma, or other pathology of the knee joint indicates cemented or cementless total knee arthroplasty.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - e1 antioxidant infused uhmwpe tibial bearing. tibial/femoral coronal conformity ratio 1.25:1. medial and lateral bearings designed independently, allowing acl/pcl interaction to drive knee motion. the vanguard xp-xp tibial bearing is intended for use as part of the vanguard xp knee system, for use with vanguard xp-xp or xp-cr tibial tray. 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 post-traumatic deformity; correction of revision of unsuccessful osteotomy, arthrodesis or failure of previous joint replacement procedure. made of e1 antioxidant infused uhmwpe.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - e1 antioxidant infused uhmwpe tibial bearing, used for an intact, partially functioning pcl. tibial/femoral coronal conformity ratio 1:1. symmetric medial and lateral articulations. the vanguard xp-as tibial bearing right medial/left lateral is intended for use as part of the vanguard xp knee system, for use with vanguard xp-xp or xp-cr tibial tray. 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 post-traumatic deformity; correction of revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. made of e1 antioxidant infused uhmwpe.

أستراليا - الإنجليزية - Department of Health (Therapeutic Goods Administration)

zimmer biomet pty ltd - 46585 - prosthesis, knee, internal, insert component - e1 antioxidant infused uhmwpe tibial bearing, for use with intact, partially functioning pcl. tibial/femoral coronal conformity ratio 1:1. symmetric medial and lateral articulations. the vanguard xp anterior stabilised (as) tibial bearing left medial/right lateral is intended for use as part of the vanguard xp knee system, for use with vanguard xp-xp or xp-cr tibial tray. 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 post-traumatic deformity; correction of revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. made of e1 antioxidant infused uhmwpe.