510(k) K161404 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Genesys Spine Apache® Lateral Lumbar Interbody Fusion System
| Applicant | Genesys Spine, Austin TX, US |
| Decision | Substantially Equivalent, Jul 21, 2016 |
| Received | May 20, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161404
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.