FDA 510(k) Applications Submitted by Jim Clossick

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040550	03/02/2004	LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
K221204	04/26/2022	Excipio SV Thrombectomy Device	Contego Medical Inc.
K221339	05/09/2022	Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection	Contego Medical Inc.
K041370	05/24/2004	LIFESTENT LP SDS BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
K023121	09/19/2002	LIFESTENT BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
K023248	09/30/2002	LIFESTENT LP SDS BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
K023308	10/03/2002	LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
K033212	10/03/2003	LIFESTENT SDS BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
K223897	12/28/2022	Excipio LV Thrombectomy Device	Contego Medical Inc.