Paradigm Spine, LLC
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K153302 | coflex-IF | PEK | 2016-09-08 | View |
| 510(k) | K120491 | DSS STABILIZATION SYSTEM-RIGID | MNH | 2012-05-09 | View |
| 510(k) | K112595 | COFLEX-F | KWP | 2012-02-13 | View |
| 510(k) | K113625 | DSS STABILIZATION SYSTEM | NKB | 2012-01-10 | View |
| 510(k) | K093438 | PARADIGM INTERSPINOUS FUSION PLATE | KWP | 2010-10-06 | View |
| 510(k) | K101083 | DSS STABILIZATION SYSTEM | NQP | 2010-07-02 | View |
| 510(k) | K091944 | MODIFICATION TO: DSS STABILIZATION SYSTEM | NQP | 2009-08-03 | View |
| 510(k) | K090099 | DSS STABILIZATION SYSTEM | NKB | 2009-06-19 | View |
| 510(k) | K090408 | MODIFICATION TO: DSS STABILIZATION SYSTEM | NKB | 2009-03-20 | View |
| 510(k) | K080241 | DDS STABILIZATION SYSTEM | NQP | 2008-11-28 | View |
| 510(k) | K072969 | DSS | NQP | 2008-01-24 | View |
No matching devices.
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