Additive Implants, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2021-07-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K211111 | SureMAX-SA Cervical Standalone System | OVE | 2021-07-16 | View |
| 510(k) | K193359 | SureMAX Family of Cervical Spacers | ODP | 2020-01-03 | View |
No matching devices.