K-number	K030526
Device name	PEDIGUARD NERVE DETECTOR SYSTEM
Applicant	Spine Vision, Inc.
Product code	GWF
Device class	Class II
Decision date	Dec 29, 2004
Decision	Substantially Equivalent
Regulation	882.1870

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View the full FDA submission: accessdata.fda.gov

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PEDIGUARD NERVE DETECTOR SYSTEM

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