K-number	K760976
Device name	CHARNLEY REVISION SET
Applicant	Codman & Shurtleff, Inc.
Product code	JDG
Device class	Class II
Decision date	Nov 16, 1976
Decision	Substantially Equivalent
Regulation	888.3360

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View the full FDA submission: accessdata.fda.gov

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CHARNLEY REVISION SET

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