FDA 510(k) Applications Submitted by LINDA GUTHRIE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K070126	01/16/2007	OCCLUSION BALLOON CATHETER	SENTREHEART INC.
K080364	02/11/2008	FINDRWIRZ GUIDE WIRE SYSTEM	SENTREHEART INC.
K090385	02/17/2009	LARIAT II SUTURE DELIVERY DEVICE	SENTREHEART INC.
K031371	04/30/2003	SAPHYRE BIPOLAR ABLATION PROBES	SMITH & NEPHEW, INC.
K032217	07/21/2003	14G CORMARK BIOPSY SITE IDENTIFIER	ARTEMIS MEDICAL, INC.
K013622	11/05/2001	NUCLEOTOMY INTRADISCAL CATHETER	ORATEC INTERVENTIONS, INC.
K003893	12/18/2000	VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL PROBES, MODEL 91000X,91002X,91300X	ORATEC INTERVENTIONS, INC.