K-number	K130548
Device name	EPICAGE INTERBODY FUSION DEVICE
Applicant	Alphatec Spine, Inc.
Product code	MAX
Device class	Class II
Decision date	Apr 18, 2013
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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EPICAGE INTERBODY FUSION DEVICE

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