FDA 510(k) Applications Submitted by F. DAVID ROTHKOPF

FDA 510(k) Number	Submission Date	Device Name	Applicant
K080575	02/29/2008	CORRIDOR4DM	INVIA
K090601	03/05/2009	FSC 2	SCHOELLY IMAGING, INC.
K050663	03/15/2005	TRAXYLOC-1 SYSTEM	TRAXYZ MEDICAL, INC.
K111576	06/06/2011	NT 2000 LESIONING GENERATOR	NEUROTHERM, INC.
K101660	06/14/2010	ECG SINGLE PATIENT USE LEAD WIRE SET, MODELS 2048801-5 TO 2048801-8	KEPLER MEDTEC
K091800	06/17/2009	LIPOEZE LASER ASSISTED ASPIRATION CANNULA	CURVE MEDICAL
K122503	08/16/2012	PARALLAX BALLOON INFLATABLE BONE TAMP-10 MM BALLOON PARALLAX BALLOON INFLATABLE BONE TAMP-15 MM BALLOON PARALLAX BALLOON	NEURO THERM, INC.
K083553	12/01/2008	NASO-LARYNGO-PHARYNGOSCOPE	SCHOELLY IMAGING, INC.
K024171	12/18/2002	VIDAR BONE TRACK SYSTEM SOFTWARE	VIDAR SYSTEMS CORP.