510(k) K211417 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
F3D-C2 Cervical Stand-Alone System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Feb 4, 2022 |
| Received | May 7, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211417
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.