BEUDAMED
    686 results · 38ms · Sources: EU EUDAMED, US FDA

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    KYPHON INC.

    FDA Adverse Event
    Malfunction ·KYPHON INC.·Product code HXG·November 17, 2004

    KYPHON INC

    FDA Adverse Event
    Other ·KYPHON, INC·Product code NDN·September 19, 2006

    BKP BALLOONS

    FDA Adverse Event
    Injury ·MDT KYPHON SUNNYVALE MFG·Product code HXG·January 19, 2021

    BKP CEMENT

    FDA Adverse Event
    Malfunction ·MDT KYPHON SUNNYVALE MFG·Product code NDN·January 19, 2021

    BKP CEMENT

    FDA Adverse Event
    Injury ·MDT KYPHON SUNNYVALE MFG·Product code NDN·January 19, 2021

    Kyphon, Functional Anaesthetic Discography (F.A.D.) Introducer Needle, Catalog Number: D01B, Kyphon, Inc., Sunnyvale, Ca 94089

    FDA Recall
    Terminated ·Kyphon Inc·Product code BSP·April 25, 2006

    KYPHX® HV-R¿ BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC.·Product code NDN·October 3, 2011

    Functional Anaesthetic Discography (F.A.D.) Catheter System, Catalog #: D01A, Kyphon, Inc., Sunnyvale, Ca 94089

    FDA Recall
    Terminated ·Kyphon Inc·Product code BSP·April 25, 2006

    Kyphon brand KyphoPak Express Tray First Fracture, 15/2 with KyphX Osteo Introducer System; Catalog Number: KPE1003; Product is manufactured and distributed by Medtronic Spine LLC (formerly known as Kyphon Inc), Sunnyvale, CA Designed to reduce kyphosis that results from vertebral body collapse due to osteoporosis.

    FDA Recall
    Terminated ·Medtronic Spine LLC (formerly Kyphon Inc.)·Product code HRX·March 23, 2011

    KHYPHON/MEDTRONICS MMPA

    FDA Adverse Event
    Injury ·KHYPHON·Product code LOD·April 4, 2003

    KYPHX INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·KYPHON, INC.·Product code HRX·May 12, 2010

    KYPHX INFLATABLE BONE TAMP

    FDA Adverse Event
    Injury ·KYPHON, INC.·Product code HRX·June 28, 2010

    KYPHX INFLATABLE BONE TAMP, 20/3

    FDA Adverse Event
    Injury ·KYPHON INC.·Product code HXG·March 19, 2004

    KYPHX BONE FILLER DEVICE

    FDA Adverse Event
    Injury ·KYPHON INC.·Product code KIH·February 20, 2004

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Death ·KYPHON, INC.·Product code NDN·February 17, 2004

    BONE FILLER DEVICE

    FDA Adverse Event
    Injury ·KYPHON INC.·Product code KIH·March 29, 2002

    INFLATABLE BONE TAMP

    FDA Adverse Event
    Injury ·KYPHON INC.·Product code HXG·February 1, 2002

    KYPHX BONE BIOSPY DEVICE

    FDA Adverse Event
    Other ·KYPHON, INC.·Product code MJG·December 15, 2003

    KYPHX 11 GAUGE BONE ACCESS NEEDLE

    FDA Adverse Event
    Injury ·KYPHON INC.·Product code GCB·September 26, 2003

    KYPHX BONE FILLER DEVICE

    FDA Adverse Event
    Injury ·KYPHON INC.·Product code KIH·July 30, 2003