Naviswiss AG
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2023-01-31
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K223351 | Naviswiss Knee | OLO | 2023-01-31 | View |
| 510(k) | K211429 | NAVIPLAN - CT Planning Software for Total Hip Replacement | LLZ | 2021-10-05 | View |
| 510(k) | K193094 | Naviswiss Hip Navigation System | OLO | 2020-06-10 | View |
No matching devices.