510(k) K133967 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INTERBODY CAGE SYSTEM
| Applicant | Aurora Spine, Washington DC, US |
| Decision | Substantially Equivalent, Jan 31, 2014 |
| Received | Dec 24, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133967
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.