510(k) K133514 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
XCAGE INTERBODY FUSION SYSTEM
| Applicant | Ouroboros Medical, Fremont CA, US |
| Decision | Substantially Equivalent, May 1, 2014 |
| Received | Nov 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133514
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.