K-number	K061640
Device name	INTEGRA MOBIUS MULTI-MODALITY MONITORING SYSTEM
Applicant	Integra LifeSciences Corporation
Product code	GWM
Device class	Class II
Decision date	Jul 27, 2006
Decision	Substantially Equivalent
Regulation	882.1620

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View the full FDA submission: accessdata.fda.gov

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INTEGRA MOBIUS MULTI-MODALITY MONITORING SYSTEM

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