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AxSOS 3 AF System and AxSOS 3 Ti System

Page Type
Cleared 510(K)
510(k) Number
K200398
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2020
Days to Decision
108 days
Submission Type
Summary

AxSOS 3 AF System and AxSOS 3 Ti System

Page Type
Cleared 510(K)
510(k) Number
K200398
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2020
Days to Decision
108 days
Submission Type
Summary