510(k) K250560 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
BEE HA
| Applicant | NGMedical GmbH, Nonnweiler, DE |
| Decision | Substantially Equivalent, Nov 21, 2025 |
| Received | Feb 25, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250560
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.