FDA 510(k) Applications Submitted by KATHY BOGGS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230295 | 02/02/2023 | ATTUNE« Revision Cones | DePuy Ireland UC |
| K101433 | 05/21/2010 | DEPUY ATTUNE KNEE SYSTEM | DEPUY ORTHOPAEDICS, INC. |
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