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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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