K-number	K142193
Device name	COGENT MED-LIF XL
Applicant	Cogent Spine, LLC
Product code	MAX
Device class	Class II
Decision date	Oct 15, 2014
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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COGENT MED-LIF XL

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