K-number	K053447
Device name	ARTHROCARE PERC-D SPINEWAND
Applicant	Arthrocare Corp.
Product code	GEI
Device class	Class II
Decision date	Dec 27, 2005
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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ARTHROCARE PERC-D SPINEWAND

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