510(k) K221128 · MAI Fastener, Fixation, Biodegradable, Soft Tissue
Arthrex ACL TightRope®, PCL TightRope®, and TightRope® II
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Oct 5, 2022 |
| Received | Apr 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221128
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.