510(k) K133418 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, May 1, 2014 |
| Received | Nov 7, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133418
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.