FDA 510(k) Applications Submitted by Sandeep Saboo

FDA 510(k) Number	Submission Date	Device Name	Applicant
K190099	01/22/2019	Veloxion Controller Kit, Veloxion Fluid Control Kit, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch	Corinth MedTech, Inc.
K190113	01/24/2019	Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags	Corinth MedTech, Inc.
K180752	03/22/2018	Veloxion System, Veloxion Controller Kit, Veloxion Resecting Device Kit, Veloxion Fluid Control Set, Veloxion Saline Pole	Corinth MedTech, Inc.
K090986	04/07/2009	STABILI ERX BONE CEMENT, MODEL 1135,STABILIT VERTEBRAL AUGMENTATION SYSTEM (FOR USE W/ STABILIT ERX BONE CEMENT)	DFINE, INC.
K091310	05/04/2009	ABLATION INSTRUMENT, MODEL 1635; ABLATION MULTIPLEX CATHETER, MODEL 1682	DFINE, INC.
K191335	05/17/2019	Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags	Corinth MedTech, Inc.
K191341	05/20/2019	Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags	Corinth MedTech, Inc.
K162979	10/26/2016	Veloxion System	Corinth MedTech, Inc.