Ossur North America Inc
7 FDA 510(k) clearances · Recalling firm
◉ Watch Ossur North America Inc
| Record | Firm | Date |
|---|---|---|
| Fixed Offset Adapter, A-642100. The Offset Adapter is a fixed modular component which sets recall (Z-0362-2014) | Ossur North America Inc | 2013-11-19 |
| Ossur Total Knee Junior, Model Number TK 1100, External Prosthetic knee. recall (Z-1197-06) | Ossur North America Inc | 2006-07-04 |
| Ossur Total Knee 1900, Model Number TK 1900, external prosthetic knee. recall (Z-1198-06) | Ossur North America Inc | 2006-07-04 |
| Ossur Total Knee 2000, Model Number TK 2000, external prosthetic knee. recall (Z-1199-06) | Ossur North America Inc | 2006-07-04 |
| Ossur Total Knee 2100, Model Number TK 2100, external prosthetic knee. recall (Z-1200-06) | Ossur North America Inc | 2006-07-04 |
| VSP Shock Module (as part of a prosthetic foot). recall (Z-1083-04) | Ossur North America Inc | 2004-07-20 |
| Mauch XG, Caron Knee Frame. Model numbers FDM01804U, FRM01804LU, FRM01851U, FRM61750. recall (Z-0815-03) | Ossur North America Inc | 2003-05-14 |
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Every clearance here is in the API, with alerts when new ones post.