510(k) K233971 ยท MAI Fastener, Fixation, Biodegradable, Soft Tissue
Arthrex AlloSync PushLock Suture Anchor
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jun 4, 2024 |
| Received | Dec 15, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233971
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.