510(k) K173453 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
Valeo® C+CSC with Lumen Interbody Fusion Device
| Applicant | Amedica Corp., Slat Lake City UT, US |
| Decision | Substantially Equivalent, Mar 5, 2018 |
| Received | Nov 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173453
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.