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FDA 510(k) Applications Submitted by Megan B Guilbault
FDA 510(k) Number
Submission Date
Device Name
Applicant
K223767
12/15/2022
Ortho Guidance Precision Knee Software, Ortho Guidance Express Knee Software, Ortho Guidance Versatile Hip Software, Ortho Q Guidance System
Stryker Leibinger GmbH & Co. KG
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