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ACTIFY™ 3D Total Knee System, ACTIFY™ Total Knee System

Page Type
Cleared 510(K)
510(k) Number
K240669
510(k) Type
Traditional
Applicant
Globus Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2024
Days to Decision
101 days
Submission Type
Summary

ACTIFY™ 3D Total Knee System, ACTIFY™ Total Knee System

Page Type
Cleared 510(K)
510(k) Number
K240669
510(k) Type
Traditional
Applicant
Globus Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2024
Days to Decision
101 days
Submission Type
Summary