FDA 510(k) Applications Submitted by icotec AG

FDA 510(k) Number	Submission Date	Device Name	Applicant
K151977	07/17/2015	icotec Pedicle System	ICOTEC AG
K200235	01/30/2020	KONG-TL VBR System, KONG-C VBR System	icotec ag
K190545	03/04/2019	VADER« one Pedicle System MIS and LightMore« Pedicle System 6.0	icotec ag
K200596	03/06/2020	G21 Cement, VADER« Pedicle System	Icotec AG
K230861	03/29/2023	VADER« Pedicle System Navigated Instruments	Icotec ag
K201587	06/11/2020	icotec Anterior Cervical Plate System	Icotec AG
K232628	08/29/2023	VADER« Pedicle System	icotec AG
K232790	09/11/2023	KONG«-TL VBR System and KONG« C VBR System	icotec AG
K232792	09/11/2023	icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurnÖ TLIF Lumbar Cage)	icotec AG
K222789	09/15/2022	VADER« Pedicle System, G21 Cement	icotec ag
K233215	09/26/2023	icotec Anterior Cervical Plate System	Icotec AG
K192897	10/11/2019	icotec Cervical Cage	icotec ag
K193423	12/09/2019	VADER«one Pedicle System MIS and LightMore« Pedicle System 6.0	Icotec AG
K172480	08/16/2017	icotec Interbody Cage System	icotec ag
K242900	09/23/2024	VADER« Pedicle System and VADER«one Pedicle System	icotec ag