K-number	K133021
Device name	MIXING SYRINGE SYSTEM
Applicant	Zimmer Knee Creations, Inc.
Product code	FMF
Device class	Class II
Decision date	Jan 13, 2014
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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MIXING SYRINGE SYSTEM

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