BEUDAMED
    131 results · 26ms · Sources: EU EUDAMED, US FDA

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    ArthroTAK, LLC

    FDA registration
    ArthroTAK, LLC·1 product·🇺🇸 United States

    ArthroTAK Tendon Anchor Kit

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTHRO+ZAK

    Device
    EU MDR · Eu Md Class 2a ·On the market

    ARTHROTAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARTHRO+ZAK TRAY

    Device
    EU MDR · Eu Md Class 2a ·On the market

    ARTHRO+ZAK TRAY

    Device
    EU MDR · Eu Md Class 2a ·On the market

    ARTHROTEK LACTONAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTHROTEK CANNULA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTHROTEK SET SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTHROTEK INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTHROTEK INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTHROTEK MENISCAL HYBRID DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    A-TAP (previously called Arthrotap)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACL/PCL MODULAR SYSTEM

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

    ARTHROTEK

    FDA Adverse Event
    Malfunction ·ARTHROTEK·Product code HRX·November 1, 2004

    BONE MULCH SCREW +5 TIP

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

    ARTHROTEK

    FDA Adverse Event
    Malfunction ·ARTHROTEK·Product code HWC·January 12, 2004

    ARTHROTEK

    FDA Adverse Event
    Malfunction ·Product code HRX·October 29, 2012

    ARTHROTEK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS, INC.·Product code HTW·January 30, 2007