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KIRSCHNER KNEE MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K961021
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/17/1997
Days to Decision
368 days

KIRSCHNER KNEE MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K961021
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/17/1997
Days to Decision
368 days