Device Classification Name |
arthroscope
|
510(k) Number |
K020761 |
Device Name |
POWER TEK II |
Applicant |
BIOMET, INC. |
56 EAST BELL DR. |
WARSAW,
IN
46581 -0587
|
|
Applicant Contact |
PATRICIA S BERES |
Correspondent |
BIOMET, INC. |
56 EAST BELL DR. |
WARSAW,
IN
46581 -0587
|
|
Correspondent Contact |
PATRICIA S BERES |
Regulation Number | 888.1100
|
Classification Product Code |
|
Date Received | 03/07/2002 |
Decision Date | 04/03/2002 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|