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AGC REVISION KNEE PROTHESIS

Page Type
Cleared 510(K)
510(k) Number
K912245
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/19/1991
Days to Decision
90 days
Submission Type
Statement

AGC REVISION KNEE PROTHESIS

Page Type
Cleared 510(K)
510(k) Number
K912245
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/19/1991
Days to Decision
90 days
Submission Type
Statement