510(k) K201677 ยท HRS Plate, Fixation, Bone
Arthrex Mesh Plates
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 2, 2020 |
| Received | Jun 19, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201677
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.