FDA 510(k) Applications Submitted by ORBUS MEDICAL TECHNOLOGIES

FDA 510(k) Number	Submission Date	Device Name	Applicant
K041032	04/21/2004	MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
K040550	03/02/2004	LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES
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
K010107	01/12/2001	R STENT BILIARY ENDOPROSTHESIS	ORBUS MEDICAL TECHNOLOGIES