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Persona® Revision Knee System (Persona Revision SoluTion™ Femoral Components)

Page Type
Cleared 510(K)
510(k) Number
K243724
510(k) Type
Traditional
Applicant
Zimmer, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
93 days
Submission Type
Summary

Persona® Revision Knee System (Persona Revision SoluTion™ Femoral Components)

Page Type
Cleared 510(K)
510(k) Number
K243724
510(k) Type
Traditional
Applicant
Zimmer, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
93 days
Submission Type
Summary