K-number	K161405
Device name	Valeo II Interbody Fusion Device System
Applicant	Amedica Corp.
Product code	MAX
Device class	Class II
Decision date	Aug 19, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Valeo II Interbody Fusion Device System

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