FDA 510(k) Applications Submitted by Danielle Jannuzzi Madureira

FDA 510(k) Number Submission Date Device Name Applicant
K220319 02/03/2022 Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System Stryker GmbH
K210582 02/26/2021 EasyClip« and EasyClip« Xpress Stryker GmbH
K222381 08/05/2022 PeriPROÖ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System Stryker GmbH
K213199 09/29/2021 Asnis« III Cannulated Screw System and Asnis« PRO Cannulated Screw System Stryker GmbH
K223772 12/16/2022 PRO Plating System, Stryker Trauma Pelvic Set (Matta) Stryker GMbH


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