510(k) K233594 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Genesys Spine 3DP AIS-C II Cervical Interbody System
| Applicant | Genesys Spine, Austin TX, US |
| Decision | Substantially Equivalent, Dec 13, 2023 |
| Received | Nov 8, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233594
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.