510(k) K183395 ยท HWC Screw, Fixation, Bone
Arthrex 2.5 mm Tenodesis Screw
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Apr 17, 2019 |
| Received | Dec 7, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183395
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.