Centinel Spine, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest Approval2018-05-08
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K173347 | STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX | MAX | 2018-05-08 | View |
No matching devices.