510(k) K190953 ยท HRS Plate, Fixation, Bone
Arthrex Minimally Invasive Ankle Fusion Plate
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Oct 16, 2019 |
| Received | Apr 11, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190953
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.