FDA 510(k) Applications Submitted by Diane Brinza

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130092	01/15/2013	SIMMETRY SACROILIAC JOINT FUSION SYSTEM	Zyga Technology, Inc.
K110512	02/23/2011	SIMMETRY SACROILIAC JOINT FUSION SYSTEM	Zyga Technology, Inc.
K050863	04/05/2005	IMAGER II ANGIOGRAPHIC CATHETER	BOSTON SCIENTIFIC CORP.
K141549	06/11/2014	SImmetry Sacroiliac Joint Fusion System	Zyga Technology, Inc.
K111801	06/27/2011	SIMMETRY(TM) SACROILIAC JOINT FUSION SYSTEM	Zyga Technology, Inc.
K151818	07/06/2015	SImmetry Sacroiliac Joint Fusion System	Zyga Technology, Inc.
K032495	08/13/2003	THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM	LIFECORE BIOMEDICAL, INC.
K032774	09/08/2003	RENOVA INTERNAL HEX IMPLANT SYSTEM	LIFECORE BIOMEDICAL, INC.
K102907	10/01/2010	SIMMETRY SACROILIAC JOINT FUSION SYSTEM	Zyga Technology, Inc.
K052783	10/03/2005	MODIFICATION TO: IQ GUIDE WIRE, MODELS 38950-XX. 38951-XX	BOSTON SCIENTIFIC CORP.
K173501	11/13/2017	Meridian Vaginal Positioning System (VPS)	Coloplast