510(k) K122936 ยท HRS Plate, Fixation, Bone
ANKLE TRAUMA SYSTEM
| Applicant | Orthopro, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Feb 28, 2013 |
| Received | Sep 24, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122936
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.