K-number	K142480
Device name	OsteoCool V-2 RF Ablation System
Applicant	Baylis Medical Company, Inc.
Product code	GEI
Device class	Class II
Decision date	Jun 16, 2015
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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OsteoCool V-2 RF Ablation System

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