FDA 510(k) Applications Submitted by DEPUY FRANCE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120174 | 01/20/2012 | DEPUT DELTA XTEND REVERSE SHOULDER | DEPUY FRANCE |
| K122442 | 08/10/2012 | DEPUY CTA REVERSE SHOULDER SYSTEM | DEPUY FRANCE |
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