K-number	K120096
Device name	MULTIFIX P KNOTLESS FIXATION DEVICE
Applicant	ArthroCare Corporation
Product code	MBI
Device class	Class II
Decision date	Mar 27, 2012
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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MULTIFIX P KNOTLESS FIXATION DEVICE

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