FDA 510(k) Applications Submitted by TRACY BICKEL JOHNSON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K060131 |
01/18/2006 |
OSS-BODIES PROXIMAL TIBIAL SLEEVE |
BIOMET MANUFACTURING CORP. |
| K070364 |
02/07/2007 |
100KGY E-POLY MAXROM ACETABULAR LINERS |
BIOMET, INC. |
| K050327 |
02/09/2005 |
E-POLY (VITAMIN E) ACETABULAR LINERS |
BIOMET, INC. |
| K060525 |
02/27/2006 |
VANGUARD REMOVABLE MOLDED POLY TIBIA |
BIOMET MANUFACTURING CORP. |
| K141331 |
05/21/2014 |
BIOMET ORTHOPAEDIC SALVAGE SYSTEM (OSS) |
BIOMET, INC. |
| K051411 |
05/31/2005 |
ARCOMXL POLYETHYLENE LINERS AND BIOLOX DELTA HEADS |
BIOMET, INC. |
| K051843 |
07/07/2005 |
COPELAND EAS HUMERAL RESURFACING HEADS |
BIOMET, INC. |
| K122160 |
07/20/2012 |
VANGUARD XP KNEE SYSTEM |
BIOMET MANUFACTURING CORP. |
| K140509 |
02/28/2014 |
BIOMET SIDE ACCESS DISTAL FEMORAL EXPANDABLE |
BIOMET MANUFACTURING LLC |
| K061433 |
05/24/2006 |
VANGUARD ANATOMIC PATELLA GROOVE (APG) / VANGUARD V GROOVE |
BIOMET MANUFACTURING, INC. |
| K151603 |
06/12/2015 |
Arcos One-piece Femoral Revision System |
Biomet, Inc. |
| K142746 |
09/24/2014 |
G7 Finned Acetabular Shell |
BIOMET MANUFACTUTING CORP. |
| K130126 |
01/17/2013 |
SIGNATURE PERSONALIZED PATIENT CARE SYSTEM - GLENOID GUIDE SYSTEM |
BIOMET, INC. |
| K070399 |
02/12/2007 |
100KGY E-POLY ACETABULAR LINERS-ADDITIONAL PROFILES |
BIOMET MANUFACTURING, INC. |
| K053505 |
12/16/2005 |
REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS |
BIOMET MANUFACTURING, INC. |
| K142814 |
09/29/2014 |
Biomet Orthopaedic Salvage System (OSSTM) - Proximal Femoral & Hybrid Tibial |
BIOMET MANUFACTURING LLC |
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