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Ortho Guidance Precision Knee Software, Ortho Guidance Express Knee Software, Ortho Guidance Versatile Hip Software, Ortho Q Guidance System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223767
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/13/2023
Days to Decision
60 days
Submission Type
Summary

Ortho Guidance Precision Knee Software, Ortho Guidance Express Knee Software, Ortho Guidance Versatile Hip Software, Ortho Q Guidance System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223767
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/13/2023
Days to Decision
60 days
Submission Type
Summary