510(k) K250764 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SpineLinc Anterior Cervical Implant System
| Applicant | Lincotek Medical, Bartlett TN, US |
| Decision | Substantially Equivalent, Dec 5, 2025 |
| Received | Mar 13, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250764
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.