510(k) K242483 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Genesys Spine AIS-C II Cervical Interbody Fusion System
| Applicant | Genesys Spine, Austin TX, US |
| Decision | Substantially Equivalent, Feb 7, 2025 |
| Received | Aug 21, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242483
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.