510(k) K202969 ยท JEY Plate, Bone
Biomet Microfixation OmniMax MMF System
| Applicant | Biomet Microfixation, Jacksonville FL, US |
| Decision | Substantially Equivalent, Aug 5, 2021 |
| Received | Sep 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202969
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.