510(k) K212450 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Keos Anterior Cervical Interbody Fusion Device System
| Applicant | Keos, Lancaster PA, US |
| Decision | Substantially Equivalent, Jun 6, 2022 |
| Received | Aug 5, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212450
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.