510(k) K133583 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070
| Applicant | Interventional Spine, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 10, 2014 |
| Received | Nov 21, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133583
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.