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Spine Guidance Software, Stryker Q Guidance System

Page Type
Cleared 510(K)
510(k) Number
K220593
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/27/2022
Days to Decision
87 days
Submission Type
Summary

Spine Guidance Software, Stryker Q Guidance System

Page Type
Cleared 510(K)
510(k) Number
K220593
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/27/2022
Days to Decision
87 days
Submission Type
Summary