Class Class II
Ortho Guidance Precision Knee Software, Ortho Guidance Express Knee Software, Ortho Guidance Versatile Hip Software, Ortho Q Guidance System (K223767)
Description
Ortho Guidance Precision Knee Software, Ortho Guidance Express Knee Software, Ortho Guidance Versatile Hip Software, Ortho Q Guidance System by Stryker Leibinger GmbH & Co KG — FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223767
Clearance Date2023-02-13
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560