K-number	K152454
Device name	HemiCAP MTP Resurfacing Hemi-Arthroplasty System
Applicant	Arthrosurface, Inc.
Product code	KWD
Device class	Class II
Decision date	Apr 11, 2016
Decision	Substantially Equivalent
Regulation	888.3730

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Source

View the full FDA submission: accessdata.fda.gov

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HemiCAP MTP Resurfacing Hemi-Arthroplasty System

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