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Apex Revision Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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