510(k) K112561 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
NUVASIVE COROENT NO-PROFILE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 13, 2012 |
| Received | Sep 2, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112561
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.