510(k) K161265 · OWI Bone Fixation Cerclage, Sublaminar
NuVasive® VersaTie System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jul 15, 2016 |
| Received | May 5, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161265
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.