510(k) K091381 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IBEX SPINAL SYSTEM
| Applicant | Ebi, L.P., Parsippany NJ, US |
| Decision | Substantially Equivalent, Aug 7, 2009 |
| Received | May 11, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091381
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.