K-number	K101139
Device name	PROSTIVA RF THERAPY MODEL 8929 HAND PIECE
Applicant	Medtronic, Inc.
Product code	KNS
Device class	Class II
Decision date	May 21, 2010
Decision	Substantially Equivalent
Regulation	876.4300

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View the full FDA submission: accessdata.fda.gov

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PROSTIVA RF THERAPY MODEL 8929 HAND PIECE

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