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KINETIS Total Knee System

Page Type
Cleared 510(K)
510(k) Number
K143635
510(k) Type
Traditional
Applicant
MAKO SURGICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2015
Days to Decision
60 days
Submission Type
Summary

KINETIS Total Knee System

Page Type
Cleared 510(K)
510(k) Number
K143635
510(k) Type
Traditional
Applicant
MAKO SURGICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2015
Days to Decision
60 days
Submission Type
Summary