FDA 510(k) Applications Submitted by MARK D WARNER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K122529 | 08/20/2012 | ZIMMER UNICOMPARTMENTAL KNEE SYSTEM VIVACIT-E ARTICULAR SURFACE | ZIMMER, INC. |
| K152494 | 09/01/2015 | Zimmer NexGen Complete Knee Solution Tibial and Femoral Augments | ZIMMER, INC. |
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