ARTHROCARE SYSTEM 2000 CONTROLLER, ARTHROCARE SYSTEM 2000 CABLE, ARTHROCARE SYSTEM 2000 FOOTSWITCH, PLASMA SCALPEL GS, C

information about

Device Classification Name

electrosurgical, cutting & coagulation & accessories

510(k) Number K001302
Device Name ARTHROCARE SYSTEM 2000 CONTROLLER, ARTHROCARE SYSTEM 2000 CABLE, ARTHROCARE SYSTEM 2000 FOOTSWITCH, PLASMA SCALPEL GS, C
Original Applicant
ARTHROCARE CORP.
595 north pastoria ave.
sunnyvale, 
CA 
94085 -2936

Original Contact bruce prothro
Regulation Number 878.4400
Classification Product Code
GEI  
Date Received 04/24/2000
Decision Date 05/30/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Traditional
Reviewed by Third Party No

Combination Product

No