510(k) K121892 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PHANTOM PLUS CERAMIC CAGE SYSTEM
| Applicant | Amedica Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Aug 24, 2012 |
| Received | Jun 29, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121892
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.