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ATTUNE Revision Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160700
510(k) Type
Traditional
Applicant
Depuy(Ireland)
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
6/10/2016
Days to Decision
88 days
Submission Type
Summary

ATTUNE Revision Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160700
510(k) Type
Traditional
Applicant
Depuy(Ireland)
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
6/10/2016
Days to Decision
88 days
Submission Type
Summary