510(k) K223140 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
AEON-C Stand Alone System
| Applicant | Dio Medical, Inc., East Norriton PA, US |
| Decision | Substantially Equivalent, Dec 20, 2022 |
| Received | Oct 4, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223140
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.