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FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-03-29
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K162693 | VertebraLINK Fusion Platform | MAX | 2017-03-29 | View |
| 510(k) | K160722 | CorticaLINK Spinal Fusion Platform | NKB | 2016-07-07 | View |
No matching devices.