FDA 510(k) Applications Submitted by WENDY SPIELBERGER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040168	01/26/2004	MODIFICATION TO GEO STRUCTURE	INTERPORE CROSS INTL.
K050861	04/05/2005	PEEK CAS	INTERPORE CROSS INTL.
K040928	04/09/2004	EXPANDABLE PEEK VBR IMPLANT	INTERPORE CROSS INTL.
K041407	05/27/2004	TITANIUM MESH IMPLANT	INTERPORE CROSS INTL.
K041449	06/01/2004	SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SEAT	INTERPORE CROSS INTL.
K031772	06/09/2003	TI FENESTRATED PLATE	INTERPORE CROSS INTL.
K041794	07/02/2004	C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM	INTERPORE CROSS INTL.
K042798	10/08/2004	C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM	INTERPORE CROSS INTL.
K043229	11/22/2004	MODIFICATION TO ALTIUS OCT SYSTEM	INTERPORE CROSS INTL.
K033961	12/22/2003	ALTIUS OCT SYSTEM	INTERPORE CROSS INTL.