BEUDAMED
    94 results · 17ms · Sources: EU EUDAMED, US FDA

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    NFix II System 150 mm, Catalog number NX60150-1 spinal fusion surgery

    FDA Recall
    Terminated ·Synthes Spine·Product code NQP·November 7, 2008

    NFix II System 200 mm, Catalog number NX60200-1. spinal fusion surgery

    FDA Recall
    Terminated ·Synthes Spine·Product code NQP·November 7, 2008

    N-Hance System 150 mm, Catalog number NH60150-1. spinal fusion surgery

    FDA Recall
    Terminated ·Synthes Spine·Product code NQP·November 7, 2008

    NFlex Stabilization System 150 mm, Catalog number NF60150-1. spinal fusion surgery

    FDA Recall
    Terminated ·Synthes Spine·Product code NPQ·November 7, 2008

    NFlex Stabilization System 200 mm, Catalog number NF60020-1. spinal fusion surgery

    FDA Recall
    Terminated ·Synthes Spine·Product code NPQ·November 7, 2008

    TI N-Hance Rod 150 mm Sterile, Catalog number 04.600.715.02S spinal fusion surgery

    FDA Recall
    Terminated ·Synthes Spine·Product code NQP·November 7, 2008

    Synthes Bone Marrow Aspiration System, Sterile, 11 gauge, 15cm needle (without side holes) Indicated for aspirating bone marrow

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code FMF·January 26, 2011

    Synthes Medullary Tubes

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code LXH·April 1, 2010

    Synthes USA, TI Synex (TM) II Central Body 84mm - 110mm, Catalog number 04.808.010. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 37mm - 52mm, Catalog number 04.808.006. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 58mm - 84mm, Catalog number 04.808.008. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 71mm - 97mm, Catalog number 04.808.009. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 17mm - 25mm, Catalog number 04.808.002. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 21mm - 29mm, Catalog number 04.808.003. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 29mm - 44mm, Catalog number 04.808.005. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 14mm - 19mm, Catalog number 04.808.001. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 25mm - 33mm, Catalog number 04.808.004. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 45mm - 71mm, Catalog number 04.808.007. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes USA, TI Synex (TM) II Central Body 97mm - 123mm, Catalog number 04.808.011. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma. To be used with Synthes supplemental internal fixation system.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code MQP·September 14, 2009

    Synthes In Situ Bender/Cutter Kit-Wide-Sterile. Catalog Number 530.521S.

    FDA Recall
    Terminated ·Synthes USA (HQ), Inc.·Product code HRS·January 6, 2010