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OMNIBotics Knee System

Page Type
Cleared 510(K)
510(k) Number
K200888
510(k) Type
Traditional
Applicant
Corin Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2020
Days to Decision
85 days
Submission Type
Summary

OMNIBotics Knee System

Page Type
Cleared 510(K)
510(k) Number
K200888
510(k) Type
Traditional
Applicant
Corin Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2020
Days to Decision
85 days
Submission Type
Summary