510(k) K211501 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Advantage-C PEEK Cervical lnterbody Fusion Device
| Applicant | Lntelivation, LLC, Saint Simons Island GA, US |
| Decision | Substantially Equivalent, Aug 24, 2021 |
| Received | May 14, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211501
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.