510(k) K153123 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Genesys Spine Apache Interbody Fusion System
| Applicant | Genesys Spine, Austin TX, US |
| Decision | Substantially Equivalent, Apr 26, 2016 |
| Received | Oct 29, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153123
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.