510(k) K241235 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
Arthrex TightRope II
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, May 29, 2024 |
| Received | May 2, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K241235
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.