BEUDAMED
    9,099 results · 44ms · Sources: EU EUDAMED, US FDA

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    STRYKER SPINE AVS PL PEEK SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Driver Assy, Male, 4 prong, for Stryker Spine (S9SPINE-CTL - Shukla Spine/ Universal Spinal Screw Removal System)

    Device
    EU MDR · Eu Md Class 1 ·S. S. White Technologies Inc/DBA Shukla Medical·On the market·4 countries

    STRYKER NAVIGATION SYSTEM-SPINE & FLUOROSCOPY MODULES

    FDA 510(k)
    FDA Class 2 ·Neurology

    Spine Guidance Software, Stryker Q Guidance System

    FDA 510(k)
    FDA Class 2 ·Neurology

    STRYKER SPINE NULOCK ANTERIOR CERVICAL PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STRYKER SPINE VLIFT VERTEBRAL BODY REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Driver Assy, 4 prong, for Radius by Stryker Spine (S9SPINE-CTL - Shukla Spine/ Universal Spinal Screw Removal System)

    Device
    EU MDR · Eu Md Class 1 ·S. S. White Technologies Inc/DBA Shukla Medical·On the market·4 countries

    Driver Assy, Female, Hexalobe, for Xia III by Stryker Spine (S9SPINE-CTL - Shukla Spine/ Universal Spinal Screw Removal System)

    Device
    EU MDR · Eu Md Class 1 ·S. S. White Technologies Inc/DBA Shukla Medical·On the market·4 countries

    Driver Assy, Male, 4 prong, for Xia by Stryker Spine (S9SPINE-CTL - Shukla Spine/ Universal Spinal Screw Removal System)

    Device
    EU MDR · Eu Md Class 1 ·S. S. White Technologies Inc/DBA Shukla Medical·On the market·4 countries

    STRYKER SPINE REFLEX TRANSLATIONAL ANTERIOR CERVICAL PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STRYKER SPINE

    FDA Adverse Event
    Malfunction ·STRYKER SPINE·Product code KWP·March 22, 2010

    STRYKER SPINE

    FDA Adverse Event
    Malfunction ·STRYKER·Product code LXH·April 6, 2005

    STRYKER SPINE

    FDA Adverse Event
    Malfunction ·STRYKER SPINE·Product code NDN·February 13, 2015

    STRYKER SPINE

    FDA Adverse Event
    Malfunction ·STYRKER·Product code NDN·February 2, 2015

    STRYKER INTERPULSE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS·Product code FQH·November 17, 2010

    SPINE CLAMP FOR SPINE NAVIGATION PACKAGE

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HAW·December 28, 2016

    STRYKER INTERVENTIONAL SPINE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS·Product code HRX·October 17, 2017

    Xia® 3 Spinal System, Stryker Spine Power Adaptor Instrument Accessory

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XIA LP MONOAXIAL SCREW 6.5 X 45MM

    FDA Adverse Event
    Injury ·STRYKER SPINE-SWITZERLAND·Product code NKB·April 13, 2016

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    FDA Adverse Event
    Malfunction ·STRYKER·Product code HTW·August 20, 2009