K-number	K973525
Device name	MAURICE WORLDWIDE SHUNT SYSTEM
Applicant	Integra Neurocare, LLC
Product code	JXG
Device class	Class II
Decision date	Dec 16, 1997
Decision	Substantially Equivalent
Regulation	882.5550

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View the full FDA submission: accessdata.fda.gov

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MAURICE WORLDWIDE SHUNT SYSTEM

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