FDA 510(k) Applications Submitted by Megan B Guilbault

FDA 510(k) Number Submission Date Device Name Applicant
K242834 09/19/2024 System 9 Sterile Battery Container Stryker Instruments
K233542 11/03/2023 Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System Stryker Leibinger GmbH & Co. KG
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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