K-number	K063652
Device name	GLOBAL AP POROUS COATED HUMERAL STEM
Applicant	DePuy Orthopaedics, Inc.
Product code	MBF
Device class	Class II
Decision date	Feb 1, 2007
Decision	Substantially Equivalent
Regulation	888.3670

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View the full FDA submission: accessdata.fda.gov

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GLOBAL AP POROUS COATED HUMERAL STEM

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