510(k) K120918 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NUVASIVE COROENT TITANIUM SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jun 28, 2012 |
| Received | Mar 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120918
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.