FDA 510(k) Applications Submitted by Rebecca Reiter
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K183113 | 11/09/2018 | DePuy Synthes Maxillofacial Portfolio - MR Conditional | Synthes (USA) Products LLC |
| K131186 | 04/25/2013 | SYNTHES 2.7MM AND 3.5MM VARIABLE ANGLE LCP MIDFOOT/HINDFOOT SYSTEM | SYNTHES (USA) PRODUCTS LLC |
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