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AGILITY ANKLE REVISION PROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K020541
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2002
Days to Decision
90 days
Submission Type
Summary

AGILITY ANKLE REVISION PROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K020541
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/2002
Days to Decision
90 days
Submission Type
Summary