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AMK MODULAR TIBIAL WEDGE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K904205
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/22/1990
Days to Decision
40 days

AMK MODULAR TIBIAL WEDGE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K904205
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/22/1990
Days to Decision
40 days