BEUDAMED
    9 results · 51ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    ALAMO T

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS LLC (DBA ALLIANCE SPINE)·Product code MAX·January 12, 2017

    NAKOMA-SL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS, LLC (DBA ALLIANCE SPINE)·Product code KWQ·January 12, 2017

    ALAMO T INTERVERTEBRAL BODY FUSION DEVICE

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS LLC (DBA ALLIANCE SPINE)·Product code MAX·October 26, 2016

    NAKOMA-SL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS LLC (DBA ALLIANCE SPINE)·Product code KWQ·January 12, 2017

    NAKOMA-SL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS LLC (DBA ALLIANCE SPINE)·Product code KWQ·January 12, 2017

    NAKOMA-SL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS, LLC (DBA ALLIANCE SPINE)·Product code KWQ·January 12, 2017

    NAKOMA-SL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS, LLC (DBA ALLIANCE SPINE)·Product code KWQ·January 11, 2017

    NAKOMA-SL ACP SYSTEM

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS LLC (DBA ALLIANCE SPINE)·Product code KWQ·May 11, 2015

    ALAMO T INTERVENTEBRAL BODY FUSION DEVICE

    FDA Adverse Event
    Malfunction ·ALLIANCE PARTNERS LLC (DBA ALLIANCE SPINE)·Product code KWQ·May 6, 2015