K-number	K112905
Device name	COMPRESS(R) SEGMENTAL HUMERAL REPLACEMENT SYSTEM
Applicant	Biomet Orthopedics, LLC
Product code	MBF
Device class	Class II
Decision date	May 24, 2012
Decision	Substantially Equivalent
Regulation	888.3670

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View the full FDA submission: accessdata.fda.gov

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COMPRESS(R) SEGMENTAL HUMERAL REPLACEMENT SYSTEM

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