FDA 510(k) Applications Submitted by VIKKI M HOFFMAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020244	01/24/2002	SYNTHES THORACOLUMBAR SPINE LOCKING PLATE (TSLP)	SYNTHES SPINE
K030377	02/05/2003	MODIFICATION TO SYNTHES CERVIFIX SYSTEM	SYNTHES (USA)
K020517	02/19/2002	SYNTHES DUAL-OPENING USS	SYNTHES (USA)
K022791	08/22/2002	SYNTHES ANTERIOR TENSION BAND (ATB) SYSTEM	SYNTHES (USA)
K022949	09/05/2002	SYNTHES USS, CLICK'X, USS VAS, DUAL-OPENING USS AND SMALL STATURE USS	SYNTHES (USA)
K002849	09/13/2000	PRECISIONEDGE-ACC, PRECISIONEDGE-ACS, PRECISIONEDGE-LSK, AND PRECISIONEDGE-CB MICROKEATOME BLADES	SURGICAL SPECIALTIES CORP.
K003015	09/27/2000	SSC'S PCL MONOFILAMENT SAS, VIOLET, COATED, MODEL TBD	SURGICAL SPECIALTIES CORP.
K023675	11/01/2002	SYNTHES CERVIFIX/ AXON	SYNTHES (USA)
K023862	11/20/2002	NORIAN XR CALCIUM PHOSPHATE BONE VOID FILLER	SYNTHES (USA)