Wenzel Spine

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250247panaSIa SI Fusion SystemJuly 9, 2025
K231076VariLift®-C Interbody Fusion SystemSeptember 27, 2023
K231807primaLOK™ SP Interspinous Fusion SystemAugust 15, 2023
K180822VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion SystemJanuary 28, 2019
K151900VariLift-L Interbody Fusion DeviceDecember 11, 2015
K131296VARILIFT-L INTERBODY FUSION DEVICESeptember 3, 2013
K120603VARILIFT -CJanuary 29, 2013
K111123VARILIFT CERVICAL INTERBODY FUSION SYSTEMDecember 8, 2011
K100820WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEMAugust 5, 2010