Camber Spine Technologies, LLC
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories4
Latest FDA decision2024-04-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232256 | Alcantara Thoracolumbar Plate System | KWQ | 2024-04-16 | View |
| 510(k) | K203503 | Camber Sacroiliac (SI) Fixation System | OUR | 2022-09-02 | View |
| 510(k) | K210595 | SPIRA-T Oblique Posterior Lumbar Spacers, SPIRA-P Posterior Lumbar Spacers | MAX | 2021-06-15 | View |
| 510(k) | K191584 | FORTICO Anterior Cervical Fixation System | KWQ | 2019-10-22 | View |
| 510(k) | K180980 | ORTHROS™ Posterior Stabilization System; ORTHROS™ MIS Posterior Stabilization System | NKB | 2018-10-27 | View |
| 510(k) | K180724 | SPIRA Open Matrix LLIF | MAX | 2018-06-25 | View |
No matching devices.