K-number	K151660
Device name	MultiFIX S Knotless Fixation System
Applicant	ArthroCare Corporation
Product code	MBI
Device class	Class II
Decision date	Jul 16, 2015
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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MultiFIX S Knotless Fixation System

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