FDA 510(k) Applications Submitted by Corin USA Limited

FDA 510(k) Number	Submission Date	Device Name	Applicant
K231172	04/25/2023	ApolloKnee	Corin USA Limited
K153725	12/28/2015	Corin TaperFit Hip Stem	CORIN USA LIMITED
K153772	12/31/2015	Corin TriFit TS Hip	CORIN USA LIMITED
K183114	11/09/2018	Corin BiPolar-i	Corin USA Limited
K212069	07/02/2021	Corin MetaFixÖ Hip Stem	Corin USA Limited
K171847	06/21/2017	Corin Optimized Positioning System (OPSÖ) Plan	Corin USA Limited
K173884	12/21/2017	Unity Total Knee System	Corin USA Limited
K183533	12/19/2018	Unity Total Knee System	Corin USA Limited
K170808	03/17/2017	Unity Total Knee System	Corin USA Limited
K191374	05/23/2019	Revival Modular Hip Stem	Corin USA Limited
K172551	08/23/2017	Trinity PLUS Acetabular Shell	Corin USA Limited
K162942	10/21/2016	Corin MetaFix Hip Stem	CORIN USA LIMITED
K153381	11/23/2015	Corin Metafix Hip Stem	Corin USA Limited
K173880	12/21/2017	Corin TriFit CF Hip Stem	Corin USA Limited
K191831	07/09/2019	MobiliT Cup	Corin USA Limited
K170359	02/06/2017	TrinityÖ Dual Mobility System	Corin USA Limited