510(k) K161405 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Valeo II Interbody Fusion Device System
| Applicant | Amedica Corp., Slat Lake City UT, US |
| Decision | Substantially Equivalent, Aug 19, 2016 |
| Received | May 20, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161405
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.