FDA 510(k) Applications Submitted by Jaime Weeks
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160700 | 03/14/2016 | ATTUNE Revision Knee System | Depuy (Ireland) |
| K160907 | 04/01/2016 | DePuy Actis DuoFix Hip Prosthesis | DEPUY (IRELAND) |
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