K-number	K122652
Device name	ARTHROCARE TURBINATOR WAND
Applicant	ArthroCare Corporation
Product code	GEI
Device class	Class II
Decision date	Jul 2, 2013
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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ARTHROCARE TURBINATOR WAND

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