510(k) K243915 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
FIX-C 3D Ti ACIF System
| Applicant | Jeil Medical Corporation, Seoul, KR |
| Decision | Substantially Equivalent, Feb 18, 2025 |
| Received | Dec 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243915
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.