K-number	K042859
Device name	KOBRA GPS FIXATION SYSTEM
Applicant	Medtronic Vertelink, Inc.
Product code	KWQ
Device class	Class II
Decision date	Nov 24, 2004
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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KOBRA GPS FIXATION SYSTEM

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