K-number	K102802
Device name	INTEGRA ELECTRODE TUNNELING NEEDLE
Applicant	Integra LifeSciences Corporation
Product code	GYC
Device class	Class II
Decision date	Nov 23, 2010
Decision	Substantially Equivalent
Regulation	882.1310

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View the full FDA submission: accessdata.fda.gov

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INTEGRA ELECTRODE TUNNELING NEEDLE

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