FDA 510(k) Applications Submitted by KURDEA LYON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220317 | 02/03/2022 | PuraPly Micronized Wound Matrix (PuraPly MZ) | Organogenesis Inc. |
| K151769 | 06/30/2015 | Anchorage 2 CP System | STRYKER GMBH |
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