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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
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