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

johnson & johnson medical pty ltd t/a depuy synthes - 48090 - press-fit shoulder humeral stem prosthesis - the global ap standard humeral stem is made of titanium, is uncoated and implantation is intended to be performed with bone cement, press fit or impaction bone grafting. the global ap standard humeral stem is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis. the global ap standard humeral stem is part of the global ap shoulder system and indicated for use in total or hemi-shoulder replacement for the treatment of: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis; 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory; 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). the global ap standard humeral stems are also indicated for hemi-shoulder replacement for the treatment of: 1. ununited humeral head fractures; 2. avascular necrosis of the humeral head. 3. rotator cuff repairs

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

johnson & johnson medical pty ltd t/a depuy synthes - 48090 - press-fit shoulder humeral stem prosthesis - the global advantage long humeral stem is uncoated and is made from titanium. implantation is intended to be performed with either bone cement, impact grafting or press-fit. it is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis as a part of a shoulder joint replacement. the global advantage long humeral stem is the humeral component of a shoulder joint replacement. it is intended for treatment of patients with osteoarthritis, traumatic arthritis, or rheumatoid arthritis. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, ununited humeral head fractures, avascular necrosis of the humeral head.

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

johnson & johnson medical pty ltd t/a depuy synthes - 48090 - press-fit shoulder humeral stem prosthesis - the global ap long humeral stem is made of titanium, is uncoated and implantation is intended to be performed with bone cement, press fit or impaction bone grafting. the global ap long humeral stem is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis. the global ap long humeral stem is part of the global ap shoulder system and indicated for use in total or hemi-shoulder replacement for the treatment of: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis; 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory; 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). the global ap long humeral stems are also indicated for hemi-shoulder replacement for the treatment of: 1. ununited humeral head fractures; 2. avascular necrosis of the humeral head. 3. rotator cuff repairs

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

johnson & johnson medical pty ltd t/a depuy synthes - 36259 - prosthesis, internal, joint, shoulder, glenoid component - the global shoulder glenoid peg is affixed to the glenoid cavity bone to replace or repair the articulating surface. the device is made of enduron polyethylene and implantation is intended to be performed with bone cement. five pegs (one central and four peripheral) provides stability for the component. the global shoulder glenoid peg is the glenoid component of a total shoulder joint replacement. total shoulder shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component).

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

johnson & johnson medical pty ltd t/a depuy synthes - 36259 - prosthesis, internal, joint, shoulder, glenoid component - the global glenoid crosslinked anchor peg is made of crosslinked polyethylene and implantation is intended to be performed with bone cement and bone paste. the global glenoid crosslinked anchor peg achieves immediate stability with the three minimally cemented peripheral pegs, and provides fixation through an interference fit of the central peg. the central peg facilitates bony integration around the flutes for increased fixation strength. the global glenoid crosslinked anchor peg is the glenoid component of a total shoulder joint prosthesis. total shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component).

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

johnson & johnson medical pty ltd t/a depuy synthes - 36259 - prosthesis, internal, joint, shoulder, glenoid component - the global glenoid crosslinked fin is affixed to the glenoid cavity bone to replace or repair the articulating surface. the device is made of moderately cross-linked polyethylene and implantation is intended to be performed with bone cement and bone paste. the global glenoid crosslinked fin is the glenoid component of total shoulder joint replacement. total shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component).

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

johnson & johnson medical pty ltd t/a depuy synthes - 39702 - coated shoulder humeral stem prosthesis - the global fx porocoat stem is made of cocr and is coated with porocoat (titanium sintered beads) intended to improve fixation and stability by promoting bone ingrowth. global fx can be used for cemented or cementless applications. global fx provides fixation within the proximal humerus and a site of attachment for a humeral head. the global fx porocoat stem is one component of total or hemi shoulder joint replacement. total shoulder or hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). hemi-shoulder replacement is also indicated for: 1. ununited humeral head fractures. 2. avascular necrosis of the humeral head. 3. rotator cuff tear arthropathy.

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

johnson & johnson medical pty ltd t/a depuy synthes - 48088 - humeral head prosthesis - the global ap humeral head is made of cobalt chrome and designed to be attached to a humeral stem prosthesis and to articulate with the natural glenoid fossa or a glenoid fossa prosthesis as part of a shoulder replacement. eccentric heads improve anatomical matching. the global ap humeral head is the humeral head component of a total or hemi shoulder joint replacement. total shoulder or hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). hemi-shoulder replacement is also indicated for: 1. ununited humeral head fractures. 2. avascular necrosis of the humeral head.

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

johnson & johnson medical pty ltd t/a depuy synthes - 39702 - coated shoulder humeral stem prosthesis - the global ap porocoat humeral stem is made of titanium and is either cemented or cementless. it is coated with porocoat which is intended to improve fixation and stability by promoting bone ingrowth. the global ap porocoat humeral stem is designed to provide fixation within the proximal humerus and a site of attachment for a humeral head prosthesis. the global ap porocoat humeral stem is the humeral component of a total or hemi shoulder joint replacement. total shoulder or hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). hemi-shoulder replacement is also indicated for: 1. ununited humeral head fractures. 2. avascular necrosis of the humeral head. 3. rotator cuff tear arthropathy.

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

johnson & johnson medical pty ltd t/a depuy synthes - 48088 - humeral head prosthesis - the global advantage humeral head is made of cobalt chrome and designed to be attached to a humeral stem prosthesis and to articulate with the natural glenoid fossa, a glenoid fossa prosthesis as part of a shoulder replacement. eccentric heads improve anatomical matching. the global advantage humeral head is the humeral head component of a total or hemi shoulder joint replacement. total shoulder or hemi-shoulder replacement is indicated for: 1. a severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. 2. fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternative methods of treatment are unsatisfactory. 3. other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. revision of a failed primary component). hemi-shoulder replacement is also indicated for: 1. ununited humeral head fractures. 2. avascular necrosis of the humeral head.