K-number	K103034
Device name	GENESYS SPINE INTERBODY FUSION SYSTEM
Applicant	Genesys Spine
Product code	MAX
Device class	Class II
Decision date	Dec 10, 2010
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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GENESYS SPINE INTERBODY FUSION SYSTEM

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