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Apex Revision Knee System

Page Type
Cleared 510(K)
510(k) Number
K163332
510(k) Type
Special
Applicant
OMNIlife science
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
149 days
Submission Type
Summary

Apex Revision Knee System

Page Type
Cleared 510(K)
510(k) Number
K163332
510(k) Type
Special
Applicant
OMNIlife science
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
149 days
Submission Type
Summary