FDA 510(k) Applications Submitted by JONATHAN SCHELL

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170725	03/09/2017	Stryker Universal Mesh	Stryker
K210861	03/23/2021	ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)	Stryker GmbH
K171152	04/20/2017	Stryker Universal Neuro III System AXS Screw	Stryker
K221346	05/09/2022	Stryker VariAx 2 MIS Calcaneus	Stryker GmbH
K151387	05/26/2015	Stryker Universal Neuro III System: UN III AXS Screw, UN III AXS Screwdriver Blade	STRYKER
K141633	06/18/2014	PRO-PICC WITH VALVE TECHNOLOGY	MEDICAL COMPONENTS INC
K161821	07/01/2016	Stryker Universal Mesh	Stryker
K152076	07/27/2015	PEEK Customized Cranial Implant, PEEK Customized Cranial Implant Priority	Stryker
K202289	08/12/2020	ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)	Stryker GmbH
K172572	08/28/2017	Stryker Upper-Face AXS screws and Mid-Face AXS screws	Stryker
K153248	11/09/2015	PEEK Customized Cranial Implant	STRYKER
K153508	12/07/2015	Stryker CMF MEDPOR Customized Implant	Stryker