K-number	K111073
Device name	SURGIVISION INC. CLEARPOINT SYSTEM
Applicant	Surgi-Vision, Inc.
Product code	ORR
Device class	Class II
Decision date	Jun 22, 2011
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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SURGIVISION INC. CLEARPOINT SYSTEM

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