FDA 510(k) Applications Submitted by CAROL A WEIDEMAN, PH.D.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990194	01/21/1999	BIOBUTTON	LINVATEC CORP.
K960962	03/11/1996	INTERFERENCE SCREW	LINVATEC CORP.
K971059	03/24/1997	UNIVERSAL DRIVE SYSTEM	LINVATEC CORP.
K961590	04/24/1996	APEX UNIVERSAL IRRIGATION SYSTEM & TWO-CONNECTION TUBING SET	LINVATEC CORP.
K981636	05/08/1998	INTEGRATED DRIVE/PUMP SYSTEM	LINVATEC CORP.
K981637	05/08/1998	INTEGRATED DRIVE/PUMP SYSTEM FOR OTOLARYNGOLOGY	LINVATEC CORP.
K981692	05/13/1998	MENISCAL REPAIR DEVICE	LINVATEC CORP.
K953954	08/22/1995	PRELOADED SOFT TISSUE ANCHOR	LINVATEC CORP.
K983186	09/11/1998	BIO-ANCHOR, PRE-LOADED BIOABSORBABLE SUTURE ANCHOR	LINVATEC CORP.
K963932	10/01/1996	PRELOADED SOFT TISSUE ANCHOR	LINVATEC CORP.
K973758	10/02/1997	BIOSCREW ABSORBABLE INTERFERENCE SREW	LINVATEC CORP.
K954682	10/11/1995	WASHER, BOLT, NUT, ORTHOPEDIC	LINVATEC CORP.
K984171	11/20/1998	ENDOPEARL	LINVATEC CORP.
K964805	11/29/1996	BIO-ANCHOR	LINVATEC CORP.
K974538	12/03/1997	MENISCAL REPAIR DEVICE	LINVATEC CORP.
K960652	02/15/1996	BIOSCREW ABSORBABLE INTERFERENCE SCREW	LINVATEC CORP.
K960940	03/08/1996	BIOSCREW ABSORBABLE INTERFERENCE SCREW	LINVATEC CORP.
K963369	08/27/1996	BIO-ANCHOR	LINVATEC CORP.
K964548	11/13/1996	APEX UNIVERSAL DRIVE SYSTEM	LINVATEC CORP.
K955486	12/01/1995	BIO-ANCHOR	LINVATEC CORP.
K960852	03/01/1996	HALL MODULAR ACETABULAR REAMER SYSTEM	LINVATEC CORP.