510(k) K110650 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ZYSTON ARC INTERBODY SPACER
| Applicant | Biomet Spine (Aka Ebi, LLC), Parsippany NJ, US |
| Decision | Substantially Equivalent, Jun 30, 2011 |
| Received | Mar 4, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110650
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.