K-number	K120121
Device name	COMPREHENSIVE REVERSE SHOULDER-MINI BASEPLATE
Applicant	Biomet, Inc.
Product code	PHX
Device class	Class II
Decision date	Feb 16, 2012
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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COMPREHENSIVE REVERSE SHOULDER-MINI BASEPLATE

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