K-number	K061259
Device name	MODIFICATION TO ARTHROCARE PERC-D SPINEWAND
Applicant	Arthrocare Corp.
Product code	GEI
Device class	Class II
Decision date	May 18, 2006
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO ARTHROCARE PERC-D SPINEWAND

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