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FDA 510(k) Applications Submitted by Amelia Kesti
FDA 510(k) Number
Submission Date
Device Name
Applicant
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
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