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KENNEDY TIBIAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K831513
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1983
Days to Decision
77 days

KENNEDY TIBIAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K831513
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1983
Days to Decision
77 days