510(k) K203180 ยท JDR Staple, Fixation, Bone
Arthrex DynaNite Nitinol Staples
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Dec 16, 2020 |
| Received | Oct 26, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203180
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.