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EVOLUTION® Knee Systems – MR Labeling, EVOLUTION® BIOFOAM® Tibial System, EVOLUTION® Revision Tibial System, EVOLUTION® Revision CCK System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180317
510(k) Type
Traditional
Applicant
Microport Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2018
Days to Decision
88 days
Submission Type
Summary

EVOLUTION® Knee Systems – MR Labeling, EVOLUTION® BIOFOAM® Tibial System, EVOLUTION® Revision Tibial System, EVOLUTION® Revision CCK System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180317
510(k) Type
Traditional
Applicant
Microport Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2018
Days to Decision
88 days
Submission Type
Summary