FDA 510(k) Applications Submitted by SEVRINA CIUCCI, RAC

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090815	03/25/2009	PERCUTANEOUS DISCECTOMY SYSTEM	LAURIMED LLC
K040832	03/31/2004	C-PORT ANASTOMOSIS SYSTEM (DEPLOYMENT SYSTEM, CLIP, ACCESSORIES), MODEL FG-000050	CARDICA, INC.
K021062	04/02/2002	CHITO-SEAL	ABBOTT VASCULAR INC.
K091818	06/18/2009	LAURIMED SPINAL INJECTION SYSTEM	LAURIMED LLC
K072261	08/14/2007	FINESSE SYSTEM	PRIMAEVA MEDICAL, INC.
K112579	09/06/2011	WILDCAT 5F GUIDEWIRE SUPPORT CATHETER	AVINGER, INC.
K113362	11/15/2011	SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS)	SPINE VIEW, INC.
K014118	12/14/2001	MODIFICATION TO SUPERCROSS CATHETER	ABBOTT VASCULAR INC.
K093866	12/17/2009	EVALVE STEERABLE GUIDE CATHETER	EVALVE INC
K113838	12/28/2011	WILDCAT CATHETER	AVINGER, INC.
K083909	12/30/2008	SPINAL INJECTION SYSTEM	LAURIMED LLC
K111704	06/17/2011	AVINGER WILDCAT 6F GUIDEWIRE SUPPORT CATHETER AND JUICEBOX	AVINGER, INC.