K-number	K123602
Device name	TM ARDIS INTERBODY SYSTEM INSERTER
Applicant	Zimmer Trabecular Metal Technology
Product code	MAX
Device class	Class II
Decision date	Mar 1, 2013
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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TM ARDIS INTERBODY SYSTEM INSERTER

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