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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 of 68 Results
ProductCode: GEI Applicant: ARTHROCARE CORP. Decision Date To: 05/03/2024
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Export all 68 Records to ExcelExport to Excel | Download Files | More About 510(k)
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arthrocare controller (system 2000 and 8000), arthrocare patient cable, foot control, power cord and wands ARTHROCARE CORP. K063538 12/01/2006
modification to arthrocare perc-d spinewand ARTHROCARE CORP. K061259 05/18/2006
arthrocare wands ARTHROCARE CORP. K060823 04/10/2006
athrocare topaz arthrowands ARTHROCARE CORP. K053567 03/06/2006
arthrocare perc-d spinewand ARTHROCARE CORP. K053447 12/27/2005
arthrocare 8000s coblator surgery system ARTHROCARE CORP. K053297 12/06/2005
arthrocare arthrowands ARTHROCARE CORP. K052686 10/05/2005
arthrocare controller, cable, foot control, power cord, wands, models h0970-02, h2000-04, h2000-05, h0970-06 ARTHROCARE CORP. K040338 03/01/2004
arthrocare arthrowands ARTHROCARE CORP. K033584 11/28/2003
arthrocare ent plasma wands ARTHROCARE CORP. K033257 10/30/2003
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