510(k) K140716 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE
| Applicant | Interventional Spine, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 24, 2014 |
| Received | Mar 21, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140716
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.