FDA 510(k) Applications Submitted by Andrea Kiefer-Schweizer

FDA 510(k) Number Submission Date Device Name Applicant
K192297 08/23/2019 APTUS Wrist Arthrodesis Plates Medartis AG
K202589 09/08/2020 APTUS Cannulated Compression Screws, APTUS headed Cannulated Compression Screws, APTUS K-Wire System Medartis AG
K192984 10/25/2019 APTUS Clavicle System Medartis AG
K193554 12/20/2019 APTUS« Forearm Shaft Plates and APTUS« Wrist 2.5 System Medartis AG
K193633 12/27/2019 APTUS« Ankle Trauma System 2.8/3.5 Medartis AG
K193639 12/27/2019 APTUS« Foot 2.8-3.5 System Medartis AG


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact