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ARTHROFLATOR

Page Type
Cleared 510(K)
510(k) Number
K865066
510(k) Type
Traditional
Applicant
F.M. WIEST USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1987
Days to Decision
117 days

ARTHROFLATOR

Page Type
Cleared 510(K)
510(k) Number
K865066
510(k) Type
Traditional
Applicant
F.M. WIEST USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1987
Days to Decision
117 days