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

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    iLink Bone Void Filler. Packaged in a double Tyvek pouch, then placed in a box. Model Number: 50-05-0010, Exp. 2010-04.

    FDA Recall
    Terminated ·Theken Spine LLC·Product code MQV·August 26, 2008

    POLYAXIAL SCREW-SOLID 8.5X75MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code KWP·March 30, 2012

    PLATE 2 LEVEL, 40MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code KWQ·March 21, 2012

    14MM ROTARY SCRAPER

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code MAX·February 16, 2012

    SCREW DRIVER

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code MNI·February 28, 2012

    PLATE 2 LEVEL, 40MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code KWQ·March 21, 2012

    LOCKING SCREW ASSEMBLY

    FDA Adverse Event
    Malfunction ·THEKEN SPINE, LLC·Product code MNI·February 22, 2012

    LOCKING SCREW ASSEMBLY

    FDA Adverse Event
    Malfunction ·THEKEN SPINE, LLC·Product code KWP·February 24, 2012

    ALIF CAGE ASSEMBLY

    FDA Adverse Event
    Malfunction ·THEKEN SPINE, LLC·Product code MAX·February 21, 2012

    ADJ. X-CONN. MEDIUM 45-60.5MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code KWP·January 27, 2012

    SPINPLATE 14MM 31X24MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE, LLC·Product code OVD·January 25, 2012

    NONE

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code KWQ·March 21, 2012

    IMPLANT 8MM 8DEG 31X24MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code MAX·February 21, 2012

    SPINPLATE 14MM 31X24MM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE, LLC·Product code OVD·January 20, 2012

    CANNULATED CURVED LENKE PROBE

    FDA Adverse Event
    Malfunction ·THEKEN SPINE, LLC·Product code KWP·January 30, 2012

    CORAL PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Other ·THEKEN SPINE LLC·Product code NKB·January 26, 2009

    MANTA RAY ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code NEW·March 9, 2010

    TETHER ANTERIOR CERVICAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE LLC·Product code KWQ·March 9, 2010

    CORAL PEDICLE SCREW SYSTEM

    FDA Adverse Event
    THEKEN SPINE LLC·Product code NKB·January 20, 2010

    CORAL PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·THEKEN SPINE, LLC·Product code NKB·January 13, 2010