Portland Orthopaedics Pty. , Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K061564 | PORTLAND CERAMIC (BIOLOX-FORTE) FEMORAL HEAD | LZO | 2006-09-01 | View |
| 510(k) | K053417 | M-COR HIP REPLACEMENT SYSTEM | LPH | 2006-07-20 | View |
| 510(k) | K051844 | EQUATOR PLUS ACETABULAR CUP SYSTEM | MAY | 2005-10-07 | View |
| 510(k) | K032641 | MODIFICATION TO: THE MARGRON HIP REPLACEMENT SYSTEM | MEH | 2004-01-20 | View |
| 510(k) | K992815 | THE MARGRON HIP REPLACEMENT SYSTEM | MEH | 2000-02-07 | View |
No matching devices.
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