FDA 510(k) Applications Submitted by Claudia De Santis

FDA 510(k) Number Submission Date Device Name Applicant
K240613 03/05/2024 APTUS Elbow Dorsal Olecranon Plates Medartis AG
K230971 04/05/2023 APTUS« 3.5 TriLock Straight Plates Medartis AG
K232144 07/19/2023 Sterile Products of the APTUS System Medartis AG
K234062 12/22/2023 APTUS Hand Scaphoid Plates Medartis AG
K232105 07/14/2023 APTUS Foot System 2.8-3.5 Medartis AG
K232251 07/28/2023 APTUS Cannulated Compression Screws Line Extension, APTUS K-Wire System Line Extension Medartis AG
K223853 12/23/2022 Medartis APTUS« Ulna Plates Medartis AG


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