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SurgTech GENOLL Total Knee System

Page Type
Cleared 510(K)
510(k) Number
K191192
510(k) Type
Traditional
Applicant
SurgTech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2019
Days to Decision
90 days
Submission Type
Summary

SurgTech GENOLL Total Knee System

Page Type
Cleared 510(K)
510(k) Number
K191192
510(k) Type
Traditional
Applicant
SurgTech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2019
Days to Decision
90 days
Submission Type
Summary