FDA 510(k) Applications Submitted by LONNIE WITHAM

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030086	01/09/2003	PALACOS R BONE CEMENT WITH GENTAMICIN	BIOMET, INC.
K100114	01/15/2010	FAT CONCENTRATION SYSTEM	BIOMET, INC.
K050210	01/28/2005	DISPOSABLE CEMENT SPACER MOLDS FOR TEMPORARY KNEE PROSTHESES	BIOMET, INC.
K010348	02/05/2001	TANTALUM BEADS - RADIOGRAPHIC MARKER	BIOMET, INC.
K030555	02/21/2003	GPS PLATELET SEPARATION KIT WITH ANTICOAGULANT ACD-A	BIOMET, INC.
K000978	03/27/2000	ANATOMIC TOTAL KNEE PROSTHESIS	BIOMET, INC.
K021071	04/02/2002	PCCS GRAFT DELIVERY SYSTEM	BIOMET, INC.
K991756	05/24/1999	3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE	BIO-RESEARCH ASSOCIATES, INC.
K021786	05/30/2002	TITANIUM ANKLE ARTHRODESIS NAIL	BIOMET, INC.
K051496	06/06/2005	COBALT BONE CEMENT	BIOMET, INC.
K051532	06/09/2005	COBALT G HV BONE CEMENT	BIOMET, INC.
K021927	06/12/2002	PLATELET CONCENTRATE SEPARATION KIT FOR CELSEP CENTRIFUGE SYSTEM	BIOMET, INC.
K141762	07/01/2014	PERFUSE PERCUTANEOUS DECOMPRESSION SYSTEM	BIOMET, INC.
K041850	07/08/2004	MEDALLION MODULAR HIP SYSTEM	BIOMET MANUFACTURING, INC.
K982953	08/24/1998	TITANIUM INTRAMEDULLARY NAILS-VARIOUS STYLES	BIOMET, INC.
K983967	11/06/1998	PEDIATRIC CANNULATED OSTEOTOMY PLATES	BIOMET, INC.
K993956	11/22/1999	TITANIUM PEDIATRIC FEMORAL NAIL	BIOMET, INC.
K013923	11/27/2001	TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER	BIOMET ORTHOPEDICS, INC.