BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    DEPUY MOTECH PEAK 3MM FIXATION ROD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODUMED MUGX

    FDA 510(k)
    FDA Class 2 ·Radiology

    MAKO SURGICAL CORP. UNICONDYLAR KNEE IMPLANT SYSTEM II

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCHITECT C4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 31, 2018

    NONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·February 22, 2013

    NAVISTAR® THERMOCOOL®

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code OAD·August 5, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 3, 2011