510(k) K202581 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
Arthrex TightRope II
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Nov 4, 2020 |
| Received | Sep 8, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202581
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.