K-number	K161742
Device name	Aequalis PerFORM Reversed, Aequalis PerFORM+ Reversed Glenoid
Applicant	Tornier, Inc.
Product code	PHX
Device class	Class II
Decision date	Nov 15, 2016
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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Aequalis PerFORM Reversed, Aequalis PerFORM+ Reversed Glenoid

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