FDA 510(k) Applications Submitted by Andrea 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
K181009	04/17/2018	APTUS CMC-I Fusion Plate System	Medartis AG
K181425	05/31/2018	APTUS« Proximal Humerus System	Medartis AG
K191636	06/19/2019	APTUS Foot System	Medartis AG
K161861	07/06/2016	APTUS« Coronoid 2.0	Medartis AG
K191848	07/10/2019	APTUS Wrist Spanning Plates 2.5	Medartis AG
K172170	07/18/2017	APTUS(R) Wrist 2.5 System	Medartis AG
K142581	09/15/2014	APTUS Foot System	MEDARTIS AG
K142906	10/06/2014	APTUS Wrist 2.5 System	MEDARTIS AG