BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    COLORADO II SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLORADO 2 SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MNH·December 4, 2009

    COLORADO II SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MNH·May 19, 2017

    COLORADO SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 17, 2016

    COLORADO II SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·July 26, 2011

    PIONEER SURGICAL NANOSS BVF-E

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NightOwl

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CUTTING LOOP

    FDA Adverse Event
    Malfunction ·ACMI NORWALK·Product code KNS·September 24, 2004

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 6, 2013

    SWARTZ 8.5F BRAIDED TRANS INTRODUCER, SL0, 63CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DYB·February 10, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014