Additive Device, Inc. (Adi) D/B/A Restor3D
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2019-11-05
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191047 | ADI TiDAL Osteotomy Wedge | PLF | 2019-11-05 | View |
| 510(k) | K191812 | ADI Cervical Interbody Fusion Device | ODP | 2019-10-24 | View |
No matching devices.