510(k) K181295 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Genesys Spine AIS-C Cervical Stand-Alone System
| Applicant | Genesys Spine, Austin Tx, US |
| Decision | Substantially Equivalent, Aug 29, 2018 |
| Received | May 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181295
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.