510(k) K230478 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Acro Composites Interbody System
| Applicant | Acro Composites, LLC, Brecksville OH, US |
| Decision | Substantially Equivalent, Oct 19, 2023 |
| Received | Feb 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230478
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.