510(k) K193345 ยท HRS Plate, Fixation, Bone
Arthrex DynaNite Compression Plate
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jul 8, 2020 |
| Received | Dec 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193345
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.