K-number	K833410
Device name	MONOSPHERICAL GLENOID PROSTH. KEEL
Applicant	Howmedica Corp.
Product code	KWS
Device class	Class II
Decision date	Nov 7, 1983
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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MONOSPHERICAL GLENOID PROSTH. KEEL

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