K-number	K121124
Device name	ARTHREX MIXING AND DELIVERY SYSTEM
Applicant	Arthrex, Inc.
Product code	FMF
Device class	Class II
Decision date	May 16, 2012
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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ARTHREX MIXING AND DELIVERY SYSTEM

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