FDA 510(k) Applications Submitted by PARADIGM SPINE, LLC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090408 |
02/18/2009 |
MODIFICATION TO: DSS STABILIZATION SYSTEM |
PARADIGM SPINE, LLC |
| K091944 |
06/30/2009 |
MODIFICATION TO: DSS STABILIZATION SYSTEM |
PARADIGM SPINE, LLC |
| K090099 |
01/15/2009 |
DSS STABILIZATION SYSTEM |
PARADIGM SPINE, LLC |
| K080241 |
01/31/2008 |
DDS STABILIZATION SYSTEM |
PARADIGM SPINE, LLC |
| K072969 |
10/22/2007 |
DSS |
PARADIGM SPINE, LLC |
| K093438 |
11/04/2009 |
PARADIGM INTERSPINOUS FUSION PLATE |
PARADIGM SPINE, LLC |
| K112595 |
09/07/2011 |
COFLEX-F |
PARADIGM SPINE, LLC |
| K153302 |
11/13/2015 |
coflex-IF |
PARADIGM SPINE, LLC |
| K120491 |
02/17/2012 |
DSS STABILIZATION SYSTEM-RIGID |
PARADIGM SPINE, LLC |
| K113625 |
12/08/2011 |
DSS STABILIZATION SYSTEM |
PARADIGM SPINE, LLC |
|
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