510(k) K170382 ยท HWC Screw, Fixation, Bone
Arthrex Compression Screws
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, May 11, 2017 |
| Received | Feb 7, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170382
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.