Global Glenoid Crosslinked Anchor Peg - Prosthesis, internal, joint, shoulder, glenoid component

Land: Australia

Språk: engelsk

Kilde: Department of Health (Therapeutic Goods Administration)

Tilgjengelig fra:

Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes

Klasse:

Class III

Produsert av:

DePuy Ireland UC Loughbeg Ringaskiddy, Co Cork Ireland

Terapeutisk område:

36259 - Prosthesis, internal, joint, shoulder, glenoid component

Indikasjoner:

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).

Autorisasjon status:

A

Autorisasjon dato:

2019-03-19