Specialty Spine Products, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K061578 | SSP VERTEBRAL BODY REPLACEMENT | MQP | 2006-12-26 | View |
| 510(k) | K060118 | SSP PEDICLE SCREW SYSTEM | MNH | 2006-06-08 | View |
No matching devices.
Advertisement