510(k) K230329 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
F3D Interbody System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 6, 2023 |
| Received | Feb 6, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230329
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.