510(k) K262595 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
VariLift-C Cervical Interbody Fusion System
| Applicant | Wenzel Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Aug 26, 2026 |
| Received | Jul 27, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262595
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.