K-number	K161190
Device name	G7 Dual Mobility System, Active Articulation System
Applicant	Biomet, Inc.
Product code	LPH
Device class	Class II
Decision date	May 26, 2016
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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G7 Dual Mobility System, Active Articulation System

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