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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
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modification to arthrocare controller, arthrocare cable, footswitch, powercord, arthrowands and spine wands ARTHROCARE CORP. K000511 03/13/2000
modification to arthrocare controller (system 2000 and 8000), arthrocare patient cable, foot control, power cord, wands ARTHROCARE CORP. K022475 10/03/2002
modification to arthrocare arthrowands ARTHROCARE CORP. K070958 04/23/2007
modification to arthrocare arthrowands ARTHROCARE CORP. K083306 12/10/2008
entec reflex wand 55, model e4055-01, e4045-01 ARTHROCARE CORP. K000778 05/03/2000
entec reflex wand 55, model e4055-00 ARTHROCARE CORP. K000036 02/04/2000
entec plasma wands ARTHROCARE CORP. K014290 03/28/2002
entec evac plasma wand ARTHROCARE CORP. K011279 07/19/2001
entec controller, entec patient cable, footswitch, powercord, plasma wand ARTHROCARE CORP. K000228 02/22/2000
athrocare topaz arthrowands ARTHROCARE CORP. K053567 03/06/2006
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