510(k) K132790 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INFIX ANTERIOR LUMBAR SYSTEM
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 20, 2013 |
| Received | Sep 6, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132790
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.