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Persona Revision Knee System

Page Type
Cleared 510(K)
510(k) Number
K191625
510(k) Type
Traditional
Applicant
Zimmer Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2019
Days to Decision
79 days
Submission Type
Summary

Persona Revision Knee System

Page Type
Cleared 510(K)
510(k) Number
K191625
510(k) Type
Traditional
Applicant
Zimmer Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2019
Days to Decision
79 days
Submission Type
Summary