510(k) K190418 · OWI Bone Fixation Cerclage, Sublaminar
NuVasive® VersaTie® System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 21, 2019 |
| Received | Feb 21, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190418
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.