510(k) K151900 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VariLift-L Interbody Fusion Device
| Applicant | Wenzel Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Dec 11, 2015 |
| Received | Jul 10, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151900
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.