510(k) K220696 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
uCerv Flux-C 3D Porous Titanium Cervical Interbody
| Applicant | Ulrich Medical USA, Chesterfield MO, US |
| Decision | Substantially Equivalent, Aug 19, 2022 |
| Received | Mar 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220696
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.