FDA 510(k) Applications Submitted by MICHELLE L MCKINLEY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K012348	07/24/2001	MAXIM RPG PS FEMORAL COMPONENT	BIOMET, INC.
K990290	01/29/1999	CRANIOFACIAL CALCIUM PHOSPHATE CERAMIC BONE FILLER	BIOMET, INC.
K990291	01/29/1999	LACTOSORB BONE PIN	BIOMET, INC.
K010560	02/26/2001	PORTRAIT FEMORAL COMPONENT	BIOMET, INC.
K000760	03/08/2000	REACH FEMORAL COMPONENT	BIOMET, INC.
K010774	03/14/2001	AVL HINGE KNEE SYSTEM	BIOMET, INC.
K011110	04/11/2001	M2A ACETABULAR SYSTEM	BIOMET, INC.
K011399	05/07/2001	BIOMET CRANIOFACIAL ACRYLIC CEMENT	BIOMET, INC.
K991763	05/24/1999	LACTOSORB HAND SYSTEM	BIOMET, INC.
K001660	05/31/2000	MALLORY HEAD MODULAR CALCAR	BIOMET ORTHOPEDICS, INC.
K991990	06/14/1999	TRI-POLAR SYSTEM	BIOMET, INC.
K992158	06/25/1999	LACTOSORB SHEETS	BIOMET, INC.
K992167	06/28/1999	PERFORMANCE KNEE SYSTEM	BIOMET, INC.
K992301	07/08/1999	REUNITE SCREWS	BIOMET MANUFACTURING, INC.
K002379	08/04/2000	M2A 28MM RINGLOC LINER	BIOMET, INC.
K002735	09/01/2000	ASCENT XXL OPEN BOX FEMORAL COMPONENT	BIOMET, INC.
K002772	09/06/2000	ASCENT XXL CLOSED BOX FEMORAL COMPONENT	BIOMET, INC.
K993438	10/12/1999	METAL ON METAL ACETABULAR SYSTEM	BIOMET, INC.
K003363	10/27/2000	M2A 32MM TAPER SYSTEM	BIOMET, INC.
K003494	11/13/2000	MIMIX BONE REPLACEMENT SYSTEM	BIOMET, INC.