K-number	K163067
Device name	CyMedica e-vive System; CY-1000
Applicant	Cymedica Orthopedics, Inc.
Product code	IPF
Device class	Class II
Decision date	Dec 1, 2016
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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CyMedica e-vive System; CY-1000

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CyMedica e-vive System; CY-1000