510(k) K200087 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
F3D Cervical Stand-Alone Interbody Fusion System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 15, 2020 |
| Received | Jan 15, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200087
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.