FDA 510(k) Applications Submitted by Amelia Kesti

FDA 510(k) Number Submission Date Device Name Applicant
K240651 03/07/2024 MRI Universal Stryker Leibinger GmbH & Co. KG
K231599 06/01/2023 Stryker MP, Mandible, HMMF and MMF AXS Screws Stryker Leibinger GmbH & Co. KG
K221855 06/27/2022 Universal CMF System Stryker Leibinger GmbH & Co. KG
K243491 11/12/2024 SternalPlate Expansion Stryker Leibinger GmbH & Co. KG


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