BEUDAMED
    838 results · 35ms · Sources: EU EUDAMED, US FDA

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    SPINAL USA INTERBODY CAGES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINAL USA VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINAL USA VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINAL USA INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINAL USA CEMENT RESTRICTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MODIFICATION TO SPINAL USA VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINAL USA ANTERIOR LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LDR SPINE USA SPINETUNE TL SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VAULT STAND ALONE ALIF SYSTEM

    FDA Adverse Event
    Malfunction ·Product code MAX·October 3, 2012

    SPINALUSA

    FDA Adverse Event
    Malfunction ·SPINAL USA·Product code KWQ·October 20, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 24, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2017

    SPINAL USA

    FDA Adverse Event
    Malfunction ·SPINAL USA·Product code HXX·October 20, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 26, 2013

    SPINAL USA RCS ANTERIOR LUMBAR BUTRESS PLATE SYSTEM, MODEL 22-1001-25

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPINAL USA TRAY / SPINAL S-LOK SCREW

    FDA Adverse Event
    Injury ·PRECISION SPINE, INC.·Product code MNI·December 26, 2019

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 12, 2013

    SPINAL USA SACRAL SCREWS

    FDA Adverse Event
    Injury ·SPINAL USA·Product code KWP·February 15, 2016