510(k) K142347 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Amedica Valeo II Interbody Fusion Device
| Applicant | Amedica Corp., Slat Lake City UT, US |
| Decision | Substantially Equivalent, Nov 18, 2014 |
| Received | Aug 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142347
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.