Navbit Pty, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-12-05
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243447 | Rapid Surgical Plan (RSP-SW-001) | LLZ | 2024-12-05 | View |
| 510(k) | K200376 | Navbit Sprint System- Supine Registration, Navbit Sprint Kit - Lateral Registration | OLO | 2020-12-10 | View |
No matching devices.