FDA 510(k) Applications Submitted by Sanja Jahr

FDA 510(k) Number	Submission Date	Device Name	Applicant
K200869	04/01/2020	Gamma3 System	Stryker Trauma GmbH
K221003	04/05/2022	Autosuture EEA Stapler / circular stapler with DST Series Technology / EEA Autosuture Circular Stapler with DST Series Technology / DST Series EEA Stapler / DST EEA	Covidien
K191412	05/28/2019	VariAx 2 System, VariAx 2 Mini Fragment System	Stryker GmbH
K161993	07/19/2016	Leva« Anterior Interbody System	Spine Wave, Inc.
K152174	08/04/2015	Sniper Spine System	SPINE WAVE, INC.
K162639	09/22/2016	ProficientÖ Posterior Cervical Spine System	Spine Wave, Inc.
K183104	11/08/2018	Mini Cannulated Headed and Headless Screw Set	Stryker GmbH
K193308	11/29/2019	T2 Alpha Tibia Nailing System, IMN Screws System	Stryker Trauma GmbH
K203568	12/07/2020	Hoffmann LRF System	Stryker GmbH