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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
 
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arthrocare cavity spinewand ARTHROCARE CORP. K063172 04/27/2007
arthrocare controller, cable, foot control, power cord, wands, models h0970-02, h2000-04, h2000-05, h0970-06 ARTHROCARE CORP. K040338 03/01/2004
arthrocare controller, model h2000; arthrocare cable, model h0970-02; footswitch, model h2000-04; powercord, model h2000 ARTHROCARE CORP. K011634 06/19/2001
arthrocare controller; arthrocare cable; foot control; power cord; wands ARTHROCARE CORP. K020557 03/21/2002
arthrocare perc-d spinewand ARTHROCARE CORP. K053447 12/27/2005
arthrocare system 15000 contoller, model 72202149, arthrocare arthrowands, model 72202139,72202141, 72202143, 72202144 ARTHROCARE CORP. K090393 06/23/2009
athrocare topaz arthrowands ARTHROCARE CORP. K053567 03/06/2006
entec controller, entec patient cable, footswitch, powercord, plasma wand ARTHROCARE CORP. K000228 02/22/2000
entec evac plasma wand ARTHROCARE CORP. K011279 07/19/2001
entec plasma wands ARTHROCARE CORP. K014290 03/28/2002
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