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AGC TOTAL KNEE PROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K833921
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1984
Days to Decision
78 days

AGC TOTAL KNEE PROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K833921
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1984
Days to Decision
78 days