510(k) K143139 ยท HRS Plate, Fixation, Bone
Arthrex Fracture System
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jan 16, 2015 |
| Received | Nov 3, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K143139
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.