K-number	K912245
Device name	AGC REVISION KNEE PROTHESIS
Applicant	Biomet, Inc.
Product code	JWH
Device class	Class II
Decision date	Aug 19, 1991
Decision	Substantially Equivalent for Some Indications
Regulation	888.3560

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View the full FDA submission: accessdata.fda.gov

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AGC REVISION KNEE PROTHESIS

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