510(k) K190670 · HRS Plate, Fixation, Bone
ORTHOLOC 2 Lapidus with Rotation System
| Applicant | Wrightmedicaltechnologyinc, Memphis TN, US |
| Decision | Substantially Equivalent, May 14, 2019 |
| Received | Mar 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190670
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.