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OMNIBotics Knee System

Page Type
Cleared 510(K)
510(k) Number
K163338
510(k) Type
Traditional
Applicant
OMNllife Science Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2017
Days to Decision
277 days
Submission Type
Summary

OMNIBotics Knee System

Page Type
Cleared 510(K)
510(k) Number
K163338
510(k) Type
Traditional
Applicant
OMNllife Science Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2017
Days to Decision
277 days
Submission Type
Summary