K-number	K063569
Device name	EQUINOXE REVERSE SHOULDER SYSTEM
Applicant	Exactech, Inc.
Product code	PHX
Device class	Class II
Decision date	Feb 23, 2007
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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EQUINOXE REVERSE SHOULDER SYSTEM

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