Spartek Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K103383 | SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM | NKB | 2011-02-17 | View |
| 510(k) | K094002 | SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM | NKB | 2010-05-07 | View |
No matching devices.
Advertisement