Medtronic Sofamor Danek, Inc.
FDA 510(k) & PMA Approved Devices — 96 products
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Total Devices96
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251193 | Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft | MQV | 2025-06-12 | View |
| 510(k) | K243706 | Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules | MQV | 2025-01-17 | View |
| 510(k) | K230716 | Robotic Graft Delivery Instruments | OLO | 2023-07-18 | View |
| 510(k) | K132897 | CLYDESDALE SPINAL SYSTEM | MAX | 2013-12-11 | View |
| 510(k) | K133216 | CRESCENT SPINAL SYSTEM | MAX | 2013-11-22 | View |
| 510(k) | K132700 | PERIMETER INTERBODY FUSION DEVICE | MAX | 2013-09-26 | View |
| 510(k) | K131888 | T2 XVBR SPINAL SYSTEM, T2 ALTITUDE EXPANDABLE CORPECTOMY DEVICE | MQP | 2013-09-23 | View |
| 510(k) | K123027 | CAPSTONE(R) SPINAL SYSTEM | MAX | 2013-07-25 | View |
| 510(k) | K122037 | ANATOMIC PEEK CERVICAL FUSION SYSTEM CORNERSTONE PSR CERVICAL FUSION SYSTEM PEEK PREVAIL CERVICAL INTERBODY DEVICE CAPST | MAX | 2013-03-22 | View |
| 510(k) | K122513 | CLEARED UNDER GRAFTON II EDBM | MBP | 2013-03-06 | View |
| 510(k) | K123691 | MAGNIFUSE BONE GRAFT (CLEARED AS GRAFTON II EDBM) | MQV | 2013-01-31 | View |
| 510(k) | K122433 | CD HORIZON SPINAL SYSTEM | NKB | 2012-09-28 | View |
| 510(k) | K122591 | CLYDESDALE SPINAL SYSTEM | MAX | 2012-09-18 | View |
| 510(k) | K121764 | CD HORIZON SPINAL SYSTEM | NKB | 2012-08-21 | View |
| 510(k) | K121191 | VERTEX RCCONSTRUCTION SYSTEM | KWP | 2012-06-29 | View |
| 510(k) | K112473 | CD HORIZON SPINAL SYSTEM | NKB | 2011-10-21 | View |
| 510(k) | K110063 | SOVEREIGN SPINAL SYSTEM | OVD | 2011-10-04 | View |
| 510(k) | K111510 | CD HORIZON SPINAL SYSTEM | NKB | 2011-09-15 | View |
| 510(k) | K102886 | CD HORIZON SPINAL SYSTEM | KWP | 2011-01-26 | View |
| 510(k) | K102807 | CD HORIZON SPINAL SYSTEM | NKB | 2010-11-17 | View |
No matching devices.
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