510(k) K170592 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
NuVasive BASE Interfixated Titanium System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Apr 26, 2017 |
| Received | Feb 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170592
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.