510(k) K092774 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ATLAS INTERVERTEBRAL BODY CAGE
| Applicant | Spinal Edge, LLC, Avon OH, US |
| Decision | Substantially Equivalent, Feb 2, 2010 |
| Received | Sep 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092774
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.