VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System — Wenzel Spine, Inc. (510(k) K180822)
VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System — Wenzel Spine, Inc. (510(k) K180822) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System; Applicant: Wenzel Spine, Inc.; Clearance track:
| Device name | VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System |
|---|---|
| Applicant | Wenzel Spine, Inc. |
| Clearance track | 510(k) |
| Submission number | K180822 |
| Decision | Substantially Equivalent |
| Decision date | 2019-01-28 |
| Date received | 2018-03-30 |
| Product code | MAX |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | TX, US |
| Source | openFDA device |
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$1999/mo
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