510(k) K123241 ยท HRS Plate, Fixation, Bone
ARTHREX FRACTURE PLATES
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Apr 5, 2013 |
| Received | Oct 17, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123241
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.