510(k) K171173 · HRS Plate, Fixation, Bone
OrthoPediatrics Titanium PediPlates® System
| Applicant | OrthoPediatrics Corp., Warsaw IN, US |
| Decision | Substantially Equivalent, Aug 24, 2017 |
| Received | Apr 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171173
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.