510(k) K140162 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AP EXPANDABLE XLIF SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 2, 2014 |
| Received | Jan 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140162
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.