Spineway
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-10-10
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231658 | VEOS Spinal Fixation System | NKB | 2023-10-10 | View |
| 510(k) | K162694 | Ayers Rock Cervical interbody fusion system | ODP | 2017-01-12 | View |
No matching devices.