510(k) K113527 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OPTICAGE INTERBODY FUSION DEVICE
| Applicant | Interventional Spine, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 20, 2012 |
| Received | Nov 30, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113527
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.