FDA 510(k) Applications Submitted by DAVID PADGETT, RAC (US)
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K090060 |
01/09/2009 |
NEXLINK OCT SYSTEM, MODEL 7000 SERIES |
ABBOTT SPINE, INC. |
K121671 |
06/06/2012 |
PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM |
ZIMMER SPINE, INC. |
K082032 |
07/17/2008 |
SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310) |
ABBOTT SPINE, INC. |
K072672 |
09/21/2007 |
SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES |
ABBOTT SPINE, INC. |
K100845 |
03/25/2010 |
PATHFINDER II, MINIMALLY INVASIE PEDICLE SCREW SYSTEM MODEL 3500 SERIES |
ZIMMER SPINE, INC |
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