510(k) K180822 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System
| Applicant | Wenzel Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Jan 28, 2019 |
| Received | Mar 30, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180822
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.