510(k) K173117 · OWI Bone Fixation Cerclage, Sublaminar
NuVasive® VersaTie System
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Dec 7, 2017 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173117
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.