510(k) K172052 ยท JDR Staple, Fixation, Bone
Arthrex DynaNite Nitinol Staple
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Dec 13, 2017 |
| Received | Jul 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172052
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.