510(k) K201132 ยท HRS Plate, Fixation, Bone
Arthrex Compression Screws
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jul 27, 2020 |
| Received | Apr 28, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201132
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.