K-number	K091196
Device name	GRS GLENOID RESURFACING SYSTEM
Applicant	Arthrosurface, Inc.
Product code	KWS
Device class	Class II
Decision date	Oct 27, 2009
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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GRS GLENOID RESURFACING SYSTEM

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