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

zimmer biomet pty ltd - 44854 - fixation nail, intramedullary, arthrodesis - these devices are intended for use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee. indications include: 1.) treatment of patients who are not candidates for total knee arthroplasty, 2.) irretrievably failed total knee arthroplasty. 3.) limb salvage in oncology surgery. 4.) trauma 5.) any other condition where there is little soft tissue or bony tissue available for support and arthrodesis is the treatment of choice.

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

zimmer biomet pty ltd - 44742 - prosthetic joint implantation kit - surgical instruments used for the implantation of biomet designed prosthetic joints. includes general and specific guide blocks , trial implants .

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

zimmer biomet pty ltd - 13563 - shield, - device designed to be used for the protection of persons, or their body parts, from hazards, including mechanical or radiation.

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

zimmer biomet pty ltd - 43168 - non-constrained polyethylene acetabular liner - e1, highly cross-linked uhmwpe and ?-tocopherol dual mobility bearing designed to fit over 22.2 and 28mm modular head with a type 1 or type 12/14 taper and may only be used with g7 cobalt chrome liners. the femoral head articulates on the inner, concave surface of the active articulation bearing. once the femoral stem contacts the active articulation bearing, a secondary motion occurs between the active articulation bearing and the cocr liners. intended for uncemented applications. the active articulation e1 (antioxidant infused technology) hip bearing is designed to fit over 22.2mm and 28mm modular heads. the modular head articulates with the active articulation e1 hip bearing, which in turn articulates with a g7 dual mobility liner inside a g7 acetabular shell, or a biomet acetabular shell. the components are intended for use with either primary or revision hip arthroplasties where all devices associated with the wear couple are removed and replaced. indications include: non-inflammatory degenerative joint disease, including osteoarthritis and avascular necrosis; rheumatoid arthritis; correction of functional deformity; treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable by other techniques; revision of previously failed total hip arthroplasty; dislocation risks. intended for uncemented applications.

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

zimmer biomet pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - cobalt chrome alloy tibial tray is for cemented use features 25 mm tapered stem boss which accepts offset stem adapters, stem extensions and cruciate wing augments. the superior surface features a cylindrical post that blends into a distal cone which is designed to mate with the vanguard da 360 tibial bearing. the seven symmetrical baseplate sizes in 4 mm m/l increments. packaged with ti/uhmwpe screw. cobalt chrome alloy tibial tray is a component of vanguard ssk 360 revision knee system. 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 - 33581 - coated hip femur prosthesis, modular - a sterile implantable principal component of a total hip prosthesis typically designed to replace the femoral head, neck, and stem.

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

zimmer biomet pty ltd - 32831 - uncoated knee femur prosthesis - reduced size resurfacing distal femoral component is utilized for basic reconstruction and larger defects of the distal femur. available in two options, which repalce either 3cm or 5cm of the distal femur. accepts any of the non-collared oss stems and may be used with any of the oss tibial options. oss rs components are used for treatment in small adults and adolescents. the rs femur utilizes an rs axle and rs poly femoral bushings. made from co-cr-mo and ti-6al-4v alloy. for cemented use. oss reduced size resurfacing femurs are part of the biomet oss orthopaedic salvage system, and is indicated for: 1.painful and disabled joint resulting from avascular necrosis, osteoarthritis, rheumatoid arthritis, or traumatic arthritis. 2. correction of varus, valgus, or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 4. ligament deficiencies. 5. tumor resections. 6. treatment of non-unions, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable using other techniques. 7. revision of previously failed total joint arthroplasty. 8. trauma.

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

zimmer biomet pty ltd - 32832 - uncoated knee tibia prosthesis, metallic - the oss hybrid poly tibial component utilize a polyethylene stem that is mechanically locked to the metallic baseplate. these components will primarily be used in adolescent patients that have an open epiphysis. manufactured from arcom uhmwpe and co-cr-mo alloy. intended for cemented use. oss hybrid poly tibias are part of the biomet oss orthopaedic salvage system, and is indicated for: 1.painful and disabled joint resulting from avascular necrosis, osteoarthritis, rheumatoid arthritis, or traumatic arthritis. 2. correction of varus, valgus, or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 4. ligament deficiencies. 5. tumor resections. 6. treatment of non-unions, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable using other techniques. 7. revision of previously failed total joint arthroplasty. 8. trauma.

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

zimmer biomet pty ltd - 34190 - uncoated hip femur prosthesis, modular - oss low profile proximal femur features a low profile design for smaller patients with 15 degrees of anteversion. replaces a minimum of 7 cm of the proximal femur. osseoti cylindrical, platform, or conical augments taper fit to the distal portion to promote biological fixation through tissue ingrowth. made from ti-6al-4v alloy. intended for uncemented use. oss low profile proximal femurs are part of the biomet oss orthopaedic salvage system, and is indicated for: 1.painful and disabled joint resulting from avascular necrosis, osteoarthritis, rheumatoid arthritis, or traumatic arthritis. 2. correction of varus, valgus, or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 4. ligament deficiencies. 5. tumor resections. 6. treatment of non-unions, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable using other techniques. 7. revision of previously failed total joint arthroplasty. 8. trauma.

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

zimmer biomet pty ltd - 48066 - knee stem - the oss splined stem is a straight splined collar stem that adds 1cm of replacement length to any segmental replacement. features a length of 120mm. manufactured from co-cr-mo and ti-6al-4v alloy. intended for cemented use. oss splined stems are part of the biomet oss orthopaedic salvage system, and is indicated for: 1.painful and disabled joint resulting from avascular necrosis, osteoarthritis, rheumatoid arthritis, or traumatic arthritis. 2. correction of varus, valgus, or posttraumatic deformity. 3. correction or revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 4. ligament deficiencies. 5. tumor resections. 6. treatment of non-unions, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable using other techniques. 7. revision of previously failed total joint arthroplasty. 8. trauma.