Aegis Spine, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories3
Latest Approval2023-01-20
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K223521 | ZESPIN SI Joint Fusion System | OUR | 2023-01-20 | View |
| 510(k) | K223719 | Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System | KWQ | 2023-01-11 | View |
| 510(k) | K221719 | ABTross ALIF Expandable Cage System | MAX | 2022-11-03 | View |
| 510(k) | K221050 | ZESPIN SI Joint Fusion System, Paeon Posterior Cervical Fixation System, Paeon Anterior Cervical Plate System, Spinema Lumbar Plate System | OUR | 2022-06-30 | View |
| 510(k) | K203531 | XYPAN Expandable Lumbar Cage System | MAX | 2021-01-29 | View |
No matching devices.