K-number	K011099
Device name	GLOBAL FX POROUS-COATED HUMERAL STEM
Applicant	DePuy Orthopaedics, Inc.
Product code	MBF
Device class	Class II
Decision date	Jul 6, 2001
Decision	Substantially Equivalent
Regulation	888.3670

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View the full FDA submission: accessdata.fda.gov

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GLOBAL FX POROUS-COATED HUMERAL STEM

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