K-number	K211991
Device name	Catalyst R1 Reverse Shoulder System
Applicant	Catalyst Orthoscience, Inc.
Product code	PHX
Device class	Class II
Decision date	Jul 28, 2021
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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Catalyst R1 Reverse Shoulder System

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