Spinal Devices, 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) | K081240 | TIGER DISCECTOMY DEVICE | HRX | 2009-02-27 | View |
| 510(k) | K083167 | PHENIX CERVICAL INTERBODY DEVICE | ODP | 2009-01-13 | View |
No matching devices.
Advertisement