510(k) K253041 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
3d Cage Cervical
| Applicant | Fims Co., Ltd., Suwon-Si, KR |
| Decision | Substantially Equivalent, Jul 23, 2026 |
| Received | Sep 22, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253041
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.