K-number	K171067
Device name	INVISION Total Ankle Revision System
Applicant	Wrightmedicaltechnologyinc
Product code	HSN
Device class	Class II
Decision date	Sep 11, 2017
Decision	Substantially Equivalent
Regulation	888.3110

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Source

View the full FDA submission: accessdata.fda.gov

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INVISION Total Ankle Revision System

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