K-number	K151900
Device name	VariLift-L Interbody Fusion Device
Applicant	Wenzel Spine, Inc.
Product code	MAX
Device class	Class II
Decision date	Dec 11, 2015
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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VariLift-L Interbody Fusion Device

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