Medtronic Sofamor Danek USA
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K214010 | Anteralign Spinal System with Titan nanoLOCK Surface Technology | MAX | 2022-04-12 | View |
| 510(k) | K170347 | CD HORIZON™ Fenestrated Screw Set | NKB | 2017-04-04 | View |
| 510(k) | K132111 | CD HORIZON SPINAL SYSTEM | NKB | 2013-08-06 | View |
| 510(k) | K131321 | CD HORIZON SPINAL SYSTEM | OSH | 2013-06-05 | View |
| 510(k) | K123978 | CAPSTONE L SPINAL SYSTEM | MAX | 2013-04-09 | View |
| 510(k) | K113642 | PERIMETER INTERBODY FUSION DEVICE | MAX | 2012-02-06 | View |
| 510(k) | K110562 | TELAMON PEEK SPINAL SYSTEM | MAX | 2011-11-09 | View |
| 510(k) | K111264 | CORNERSTONE (R) PSR CERVICAL FUSION SYSTEM | ODP | 2011-10-12 | View |
No matching devices.
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