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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