Device Classification Name |
electrosurgical, cutting & coagulation & accessories
|
510(k) Number |
K000511 |
Device Name |
MODIFICATION TO ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, ARTHROWANDS AND SPINE WANDS |
Applicant |
ARTHROCARE CORP. |
595 NORTH PASTORIA AVE. |
SUNNYVALE,
CA
94085 -2936
|
|
Applicant Contact |
BRUCE PROTHRO |
Correspondent |
ARTHROCARE CORP. |
595 NORTH PASTORIA AVE. |
SUNNYVALE,
CA
94085 -2936
|
|
Correspondent Contact |
BRUCE PROTHRO |
Regulation Number | 878.4400
|
Classification Product Code |
|
Date Received | 02/16/2000 |
Decision Date | 03/13/2000 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|