K-number	K141920
Device name	Wrist Hemiarthroplasty System
Applicant	Arthrosurface, Inc.
Product code	KWN
Device class	Class II
Decision date	Dec 23, 2014
Decision	Substantially Equivalent
Regulation	888.3750

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Source

View the full FDA submission: accessdata.fda.gov

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Wrist Hemiarthroplasty System

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