Global Orthopaedic Technology, USA, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K050473 | RBK PATELLA FEMORAL KNEE | KRR | 2005-11-14 | View |
| 510(k) | K051721 | GLOBAL RESURFACING UNICOMPARTMENTAL KNEE SYSTEM | HRY | 2005-10-26 | View |
| 510(k) | K033351 | GLOBAL RESURFACING UNICOMPARTMENTAL (GRU) KNEE | HRY | 2004-03-11 | View |
No matching devices.
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