510(k) K163044 · HRS Plate, Fixation, Bone
ORTHOLOC® 3Di Ankle Fracture Plating System
| Applicant | Wrightmedicaltechnologyinc, Memphis TN, US |
| Decision | Substantially Equivalent, Jan 26, 2017 |
| Received | Oct 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163044
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.