510(k) K250335 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
IVA & AEON Cervical and Lumbar Cage System
| Applicant | K&J Consulting, Lansdale PA, US |
| Decision | Substantially Equivalent, Aug 29, 2025 |
| Received | Feb 5, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250335
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.