FDA 510(k) Applications Submitted by FRED MCCLURE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K030079 |
01/09/2003 |
VERSYS BEADED FULLCOAT BOWED REVISION HIP PROSTHESIS |
ZIMMER, INC. |
| K000334 |
02/03/2000 |
IMPACT MODULAR TOTAL HIP SYSTEM |
BIOMET, INC. |
| K000335 |
02/03/2000 |
MALLORY-HEAD MODULAR CALCAR TOTAL HIP SYSTEM |
BIOMET, INC. |
| K000683 |
02/29/2000 |
MODIFIED SINGLE AXLE TOTAL ELBOW |
BIOMET, INC. |
| K991298 |
04/15/1999 |
BONE MULCH SCREW SYSTEM |
BIOMET, INC. |
| K991585 |
05/07/1999 |
BIPOLAR SHOULDER PROSTHESIS |
BIOMET, INC. |
| K991753 |
05/24/1999 |
MAXIM REMOVABLE MOLDED POLY TIBIA |
BIOMET, INC. |
| K001733 |
06/07/2000 |
ALLEN MEDULLARY CEMENT PLUGS, ZIMMER POLY PLUG INTRAMEDULLARY SYSTEM, MODEL 8011 SERIES & 1109 & 8109 SERIES |
ZIMMER, INC. |
| K021891 |
06/07/2002 |
ZIMMER TRABECULAR METAL MODULAR ACETABULAR SYSTEM |
ZIMMER, INC. |
| K981996 |
06/08/1998 |
TITANIUM FEMORAL COMPONENT |
BIOMET, INC. |
| K982398 |
07/10/1998 |
BIOMET 100% POROUS COATED BIAXIAL TOTAL ELBOW |
BIOMET, INC. |
| K983036 |
08/31/1998 |
SINGLE AXLE TOTAL ELBOW |
BIOMET, INC. |
| K993025 |
09/09/1999 |
MODIFICATION TO BONE MULCH SCREW SYSTEM |
BIOMET, INC. |
| K983641 |
10/16/1998 |
HOLLAND FEMORAL NAIL SYSTEM |
BIOMET, INC. |
| K993510 |
10/18/1999 |
MODIFIED BMP TROCHANTERIC PLATES |
BIOMET, INC. |
| K983710 |
10/21/1998 |
150MM COCR BIMETRIC HEAD/NECK REPLACEMENT HIP STEM- COLOR BUFF FINISH |
BIOMET, INC. |
| K984154 |
11/19/1998 |
APF POROUS COATED LINE EXTENSION |
BIOMET, INC. |
| K994038 |
11/29/1999 |
MODULAR REACH HIP |
BIOMET, INC. |
| K984623 |
12/30/1998 |
MAXIM REMOVABLE MOLDED POLY TIBIA |
BIOMET, INC. |
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