K-number	K093163
Device name	INTEGRA TOTAL WRIST FUSION SYSTEM
Applicant	Integra LifeSciences Corporation
Product code	HRS
Device class	Class II
Decision date	Dec 15, 2009
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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INTEGRA TOTAL WRIST FUSION SYSTEM

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