BEUDAMED
    119 results · 54ms · Sources: EU EUDAMED, US FDA

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    LOCK-SCREW, REFORM PEDICLE SCRW SYSTEM

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·April 16, 2013

    POLYAXIAL SCREWDRIVER, LOCKING

    FDA Adverse Event
    Malfunction ·SPINAL USA, INC.·Product code HXX·June 20, 2013

    VOLT INSERTER GATOR SQUID INTECH GREEN

    FDA Adverse Event
    Malfunction ·SPINAL USA, INC·Product code KWQ·September 11, 2012

    VOLT INSERTER GATOR SQUID INTECH GREEN

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code KWQ·August 16, 2012

    5.5MM X 45MM S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·July 30, 2013

    S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·July 30, 2013

    5.5 MM X 45 MM S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC.·Product code MNI·July 2, 2013

    S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·July 30, 2013

    SLIMPLICITY ANTERIOR CERVICAL PLATE 4-LEVEL 69

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code KWQ·July 30, 2013

    PSS TAPS, POWER 4.5MM

    FDA Adverse Event
    Injury ·SPINAL USA, INC.·Product code LXH·September 16, 2013

    6.5MM X 50MM S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC.·Product code MNI·July 2, 2013

    6.5 MM X 45 MM S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC.·Product code MNI·July 2, 2013

    SLIMPLICITY ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code KWQ·August 22, 2013

    6.5MM X 45MM S-LOK CANN POLY SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·September 12, 2013

    6.5MM X 40MM S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·August 23, 2013

    REFORM POLYAXIAL DRIVER

    FDA Adverse Event
    Malfunction ·SPINAL USA, INC·Product code LXH·September 23, 2013

    TPLIF OBLIQUE SIZER 5 DEGRE 8MM

    FDA Adverse Event
    Injury ·SPINAL USA, INC.·Product code LXH·August 23, 2013

    REFORM POLYAXIAL DRIVER

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code LXH·September 10, 2013

    REFORM POLYAXIAL DRIVER

    FDA Adverse Event
    Injury ·SPINAL USA INC·Product code LXH·November 15, 2013

    4.5MM X 25MM S-LOK POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·SPINAL USA, INC·Product code MNI·November 12, 2013