510(k) K232742 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
Arthrex FiberTak Suture Anchor
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Nov 3, 2023 |
| Received | Sep 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232742
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.