510(k) K192582 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
NuVasive CoRoent Small Interlock System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 13, 2019 |
| Received | Sep 19, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192582
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.