510(k) K140479 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
COROENT XL-F SYSTEM
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jul 28, 2014 |
| Received | Feb 26, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140479
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.