510(k) K242303 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
MOD-C
| Applicant | Orthomod, LLC, Dayton OH, US |
| Decision | Substantially Equivalent, Apr 1, 2026 |
| Received | Aug 5, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242303
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.