510(k) K102547 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
COROENT INTERLOCK SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Feb 7, 2011 |
| Received | Sep 3, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102547
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.