510(k) K091278 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VALEO SPACER SYSTEM
| Applicant | Amedica Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jan 28, 2010 |
| Received | May 1, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091278
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.