510(k) K260850 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
OSTEOMNI SPINAL CAGES SYSTEM
| Applicant | Osteomni, Inc., Medley FL, US |
| Decision | Substantially Equivalent, May 12, 2026 |
| Received | Mar 16, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260850
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.