K-number	K161189
Device name	Integra TITAN Reverse Shoulder System
Applicant	Integra LifeSciences Corporation
Product code	PHX
Device class	Class II
Decision date	Aug 25, 2016
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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Integra TITAN Reverse Shoulder System

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