FDA 510(k) Applications Submitted by SARAH HOLTGREWE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K080295 |
02/04/2008 |
CHARLOTTE CLAW 3.5 |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K110360 |
02/08/2011 |
PROPHECY INBONE PRE-OPERATIVE NAVIGATION ALIGNMENT GUIDES |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K120802 |
03/16/2012 |
ORTHOLOC(TM) 3DI LOCKING SCREWS ORTHOLOC(TM) BONE SCREWS |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K131143 |
04/23/2013 |
TRELLIS COLLAGEN RIBBON |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K091243 |
04/28/2009 |
ORTHOLOC ANKLE PLATING SYSTEM (APS) |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K081374 |
05/16/2008 |
CHARLOTTE LISFRANC BONE SCREW, CHARLOTTE LISFRANC PLATE |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K082320 |
08/13/2008 |
DARCO SMALL SCREW |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K102324 |
08/17/2010 |
ENDOFUSE INTRA-OSSEOUS FUSION SYSTEM |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K093405 |
11/02/2009 |
PROPHECY PRE-OPERATIVE NAVIGATION ALIGNMENT GUIDES |
WRIGHT MEDICAL TECHNOLOGY, INC. |
| K103598 |
12/08/2010 |
PROPHECY PRE-OPERATIVE NAVIGATION ALIGNMENT GUIDES |
WRIGHT MEDICAL TECHNOLOGY, INC. |
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