Device Classification Name |
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
More FDA Info for this Device |
510(K) Number |
K020905 |
Device Name |
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite |
Applicant |
BIOMET ORTHOPEDICS, INC.
P.O. BOX 587
WARSAW, IN 46581-0587 US
Other 510(k) Applications for this Company
|
Contact |
PATRICIA SANDBORN BERES
Other 510(k) Applications for this Contact |
Regulation Number |
888.3030
More FDA Info for this Regulation Number |
Classification Product Code |
LXT
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
03/20/2002 |
Decision Date |
04/15/2002 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
OR - Orthopedic |
Review Advisory Committee |
OR - Orthopedic |
Statement / Summary / Purged Status |
Summary |
Type |
Special |
Reviewed By Third Party |
N |
Expedited Review |
|