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Arthrex iBalance TKA System

Page Type
Cleared 510(K)
510(k) Number
K152252
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2015
Days to Decision
98 days
Submission Type
Summary

Arthrex iBalance TKA System

Page Type
Cleared 510(K)
510(k) Number
K152252
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2015
Days to Decision
98 days
Submission Type
Summary