Aurora Spine, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories5
Latest FDA decision2022-10-03
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221047 | SILO TFX MIS Sacroiliac Joint Fixation System | OUR | 2022-10-03 | View |
| 510(k) | K221399 | ZIP™ MIS Interspinous Fusion System | PEK | 2022-07-08 | View |
| 510(k) | K220610 | SOLO-L | OVD | 2022-05-27 | View |
| 510(k) | K210521 | DEXA-C Cervical Interbody System | ODP | 2021-08-02 | View |
| 510(k) | K210325 | APOLLO Anterior Cervical Plate (ACP) System | KWQ | 2021-03-23 | View |
No matching devices.