FDA 510(k) Applications Submitted by Wenzel Spine, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K180822 03/30/2018 VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System Wenzel Spine, Inc.
K151900 07/10/2015 VariLift-L Interbody Fusion Device WENZEL SPINE, INC.
K131296 05/06/2013 VARILIFT-L INTERBODY FUSION DEVICE WENZEL SPINE, INC.
K231076 04/14/2023 VariLift«-C Interbody Fusion System Wenzel Spine, Inc.
K231807 06/20/2023 primaLOKÖ SP Interspinous Fusion System Wenzel Spine, Inc.


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