510(k) K092901 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EPICAGE INTERBODY FUSION DEVICE
| Applicant | R Tree Innovations, Apple Valley MN, US |
| Decision | Substantially Equivalent, Apr 28, 2010 |
| Received | Sep 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092901
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.