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AMK LANDMARK REVISION KNEE FULL WEDGE TIBIAL TRAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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