Axis Orthopaedics
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest Approval2018-11-16
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K181140 | Axis Chena Cervical PEEK Spacer System | ODP | 2018-11-16 | View |
| 510(k) | K180301 | AXIS 5.5 Lumbar Pedicle Screw System | NKB | 2018-04-10 | View |
| 510(k) | K173867 | Axis Anterior Cervical Plate System | KWQ | 2018-04-05 | View |
No matching devices.