K-number	K151406
Device name	Cogent Lateral Interbody System
Applicant	Cogent Spine, LLC
Product code	MAX
Device class	Class II
Decision date	Feb 25, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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Cogent Lateral Interbody System

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