K-number	K081729
Device name	MODIFICATION TO GFX NERVE ABLATION SYSTEM
Applicant	Bioform Medical, Inc.
Product code	GXD
Device class	Class II
Decision date	Aug 7, 2008
Decision	Substantially Equivalent
Regulation	882.4400

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO GFX NERVE ABLATION SYSTEM

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