510(k) K240090 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue
Argo Knotless GENESYS Anchor
| Applicant | Conmed Corporation, Utica NY, US |
| Decision | Substantially Equivalent, Mar 5, 2024 |
| Received | Jan 12, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240090
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.