Southern Spine, LLC
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K211845 | Deploy Expandable Interbody System | MAX | 2021-11-16 | View |
| 510(k) | K130948 | C-FUSE CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM | ODP | 2013-08-14 | View |
| 510(k) | K123093 | STABILINK MIS SPINAL FIXATION SYSTEM | KWP | 2012-12-20 | View |
| 510(k) | K063764 | SOUTHERN SPINE ANTERIOR CERVICAL STABILIZATION SYSTEM, KWIK- FIX CERVICAL SYSTEM, AND KWIK-FIX / TS CERVICAL SYSTEM | KWQ | 2007-05-16 | View |
No matching devices.
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