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INVISION Total Ankle Revision System

Page Type
Cleared 510(K)
510(k) Number
K180730
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2018
Days to Decision
113 days
Submission Type
Summary

INVISION Total Ankle Revision System

Page Type
Cleared 510(K)
510(k) Number
K180730
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2018
Days to Decision
113 days
Submission Type
Summary