K-number	K131981
Device name	CEZANNE II INTERBODY FUSION SYSTEM
Applicant	Accel Spine
Product code	MAX
Device class	Class II
Decision date	Oct 9, 2013
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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CEZANNE II INTERBODY FUSION SYSTEM

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