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AMK LANDMARK REVISION KNEE FULL WEDGE TIBIAL TRAY

Page Type
Cleared 510(K)
510(k) Number
K925837
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/7/1994
Days to Decision
415 days
Submission Type
Summary

AMK LANDMARK REVISION KNEE FULL WEDGE TIBIAL TRAY

Page Type
Cleared 510(K)
510(k) Number
K925837
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/7/1994
Days to Decision
415 days
Submission Type
Summary