Medtronic Sofamor Danck USA, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K112444 | ANATOMIC PEEK CERVICAL FUSION SYSTEM | ODP | 2011-11-15 | View |
| 510(k) | K110070 | TSRH SPINAL SYSTEM | NKB | 2011-06-08 | View |
No matching devices.
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