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FDA 510(k) Applications Submitted by BECKINAM NOWATZKE
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.
K102265
08/10/2010
LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM
LDR SPINE USA
K102331
08/17/2010
LDR SPINE USA SPINETUNE TL SPINAL SYSTEM
LDR SPINE USA
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