Ortho Development
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111965 | VUSION(R) OS | MAX | 2011-10-25 | View |
| 510(k) | K111936 | ORTHO DEVLOPMENT CERAMIC FEMORAL HEAD | LZO | 2011-09-21 | View |
| 510(k) | K103837 | BALANCED KNEE SYSTEM REVISION OFFSET TIBIA | JWH | 2011-03-24 | View |
| 510(k) | K103384 | ESCALADE ACETABULAR CUP SYSTEM | LPH | 2011-03-16 | View |
No matching devices.
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