BEUDAMED
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    C-FLEX URETERAL STENTS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Monolith

    FDA UDI
    Nuvasive, Inc.·00887517676924·Monolith Core, Ø12x19mm

    DEL MAR MONOAXIAL PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNILITH PULSE GENERATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ZEPHIR ANTERIOR CERVICAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·March 6, 2013

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·February 15, 2011

    ENRHYTHM MRI

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·August 8, 2014