FDA 510(k) Applications Submitted by SHANNON SPRINGER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K081394	05/19/2008	PTFE INTERLOCK PEELABLE INTRODUCERS	ENPATH MEDICAL, INC.
K061843	06/30/2006	VENTURE WIRE CONTROL CATHETER, MODEL WCC	ST. JUDE MEDICAL
K093232	10/14/2009	OPTISEAL ENPATH VALVED PTFE PEELABLE INTRODUCER	Greatbatch Medical
K063638	12/07/2006	MODIFICATION TO PROXIS SYSTEM, MODEL EPS 101	ST. JUDE MEDICAL