Precision Spine
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2020-05-19
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K200303 | Reform Pedicle Screw System | NKB | 2020-05-19 | View |
| 510(k) | K192494 | NexGen Anterior Cervical Plate System | KWQ | 2019-10-29 | View |
No matching devices.