510(k) K203834 ยท HRS Plate, Fixation, Bone
Arthrex Patella SuturePlates
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 25, 2021 |
| Received | Dec 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203834
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.