K-number	K935802
Device name	SELECT(R) SHOULDER ALL POLY GLENOID
Applicant	Intermedics Orthopedics
Product code	KWS
Device class	Class II
Decision date	May 22, 1995
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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SELECT(R) SHOULDER ALL POLY GLENOID

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