510(k) K182361 ยท HWC Screw, Fixation, Bone
Arthrex Compression FT Screws
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Dec 18, 2018 |
| Received | Aug 30, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182361
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.