FDA 510(k) Applications Submitted by LAURA D SENEFF

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990524	02/19/1999	E9000 SYSTEM	LINVATEC CORP.
K990770	03/09/1999	BIORC ANCHOR	LINVATEC CORP.
K991024	03/29/1999	BONE BULLET SUTURE ANCHOR	LINVATEC CORP.
K991715	05/20/1999	BIOSTINGER-V BIOABSORBABLE MENISCAL REPAIR DEVICE	LINVATEC CORP.
K991830	05/28/1999	CAPSULAR SHRINKAGE ELECTRODE	LINVATEC CORP.
K993339	10/05/1999	ENDOPEARL WITH THREADER	LINVATEC CORP.
K993885	11/16/1999	ULTRABLATOR ELECTRODE	LINVATEC CORP.
K020377	02/05/2002	PRE-LOADED BIOSTINGER HORNET	LINVATEC CORP.
K030720	03/07/2003	ULTRABLATOR ELECTRODE	LINVATEC CORP.
K031098	04/07/2003	3-CCD DIGITAL CAMERA SYSTEM	LINVATEC CORP.
K002088	07/11/2000	SHAVER ABLATOR	LINVATEC CORP.
K012320	07/23/2001	POWERPRO BATTERY SYSTEM	LINVATEC CORP.
K002523	08/15/2000	ADVANTAGE DRIVE SYSTEM	LINVATEC CORP.
K022827	08/26/2002	ULTRAFIX KNOTLESS MINIMITE SUTURE ANCHOR	LINVATEC CORP.
K013117	09/18/2001	RESECTION ABLATOR	LINVATEC CORP.
K013131	09/19/2001	BIOSCREW XTRALOK	LINVATEC CORP.
K013369	10/11/2001	RESECTION ABLATOR	LINVATEC CORP.
K983652	10/19/1998	ABLATOR ELECTRODE	LINVATEC CORP.
K013553	10/25/2001	PRE-LOADED ULTRAFIX RC	LINVATEC CORP.
K003984	12/26/2000	SUPER REVO SUTURE ANCHOR	LINVATEC CORP.