510(k) K231076 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
VariLift®-C Interbody Fusion System
| Applicant | Wenzel Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Sep 27, 2023 |
| Received | Apr 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231076
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.