BEUDAMED
    17 results · 45ms · Sources: EU EUDAMED, US FDA

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    ARTHROTEK, INC

    FDA Adverse Event
    Malfunction ·BIOMET·Product code HWC·September 13, 2007

    BONE MULCH SCREW +5 TIP

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code HWC·February 12, 2004

    CURVTEK CARTRIDGE 12MM LARGE

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code GFG·January 31, 2006

    CURVTEK CARTRIDGE 12MM LARGE

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code GFG·February 22, 2006

    WASHERLOC CANCELLOUS SCREW

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code HWC·March 31, 2006

    CANNULATED HEX SCREWDRIVER 2.5MM

    FDA Adverse Event
    Malfunction ·ARTHROTEK, INC.·Product code HXX·November 22, 2006

    ARTHROTEK CANNULATED SCREWDRIVER

    FDA Adverse Event
    Malfunction ·ARTHROTEK, INC.·Product code HXX·August 15, 2002

    ANCHOR ACTOSCREW WHITE MAXBRAID

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code HWC·November 13, 2007

    ACL/PCL MODULAR SYSTEM

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code HRX·April 1, 2004

    PUMP/SHAVER CHASSIS

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code HRX·March 16, 2001

    CURVTEK CARTRIDGE 12MM LARGE

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code GFG·February 22, 2006

    SUTURE ANCHOR

    FDA Adverse Event
    ARTHROTEK INC.·Product code KGS·July 5, 1995

    BONEMULCH/WASHERLOC DISP. KIT

    FDA Adverse Event
    Injury ·ARTHROTEK, INC.·Product code HTZ·April 18, 2002

    CANNULATED SCREWDRIVER

    FDA Adverse Event
    Injury ·ARTHROTEK/BIOMET, INC.·Product code HXX·December 26, 1996

    TI-SCREW ANCHOR

    FDA Adverse Event
    Other ·ARTHROTEK/BIOMET, INC.·Product code HWC·May 15, 2006

    GENTLE THREADS ROUND HEAD SCREW

    FDA Adverse Event
    Malfunction ·ARTHROTEK/BIOMET, INC.·Product code HWC·May 16, 2008

    HARPOON SUTURE ANCHOR

    FDA Adverse Event
    Injury ·BIOMET, INC., DISTRIBUTED BY ARTHROTEK·Product code KGS·May 29, 1997