510(k) K180056 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Genesys Spine AIS-C Cervical Anchored Interbody System
| Applicant | Genesys Spine, Austin Tx, US |
| Decision | Substantially Equivalent, Mar 28, 2018 |
| Received | Jan 8, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180056
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.