K-number	K131242
Device name	ARDIS INTERBODY SYSTEM
Applicant	Zimmer Spine, Inc.
Product code	MAX
Device class	Class II
Decision date	Sep 3, 2013
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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ARDIS INTERBODY SYSTEM

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