510(k) K151732 ยท HRS Plate, Fixation, Bone
Arthrex Fracture Plates
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Aug 28, 2015 |
| Received | Jun 26, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151732
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.