K-number	K122391
Device name	MEDTRONIC XOMED, INC.
Applicant	Medtronic Xomed, Inc.
Product code	LRK
Device class	Class II
Decision date	Jan 10, 2013
Decision	Substantially Equivalent
Regulation	872.5570

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View the full FDA submission: accessdata.fda.gov

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MEDTRONIC XOMED, INC.

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