K-number	K070958
Device name	MODIFICATION TO ARTHROCARE ARTHROWANDS
Applicant	Arthrocare Corp.
Product code	GEI
Device class	Class II
Decision date	Apr 23, 2007
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO ARTHROCARE ARTHROWANDS

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