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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