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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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