510(k) K143518 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Valeo Spacer System and Valeo II Interbody Fusion Device System
| Applicant | Amedica Corp., Slat Lake City UT, US |
| Decision | Substantially Equivalent, Oct 2, 2015 |
| Received | Dec 12, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143518
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.