510(k) K143749 ยท HRS Plate, Fixation, Bone
Arthrex Distal Radius System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Apr 3, 2015 |
| Received | Dec 31, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143749
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.