BEUDAMED
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    KWA

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·June 3, 2015

    TI LOW PROFILE SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 25, 2015

    TI LOW PROFILE SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 26, 2015

    K-Wire, Blunt Sharp Tip, L=335, Ø1.7mm KWA

    FDA UDI
    PREMIA SPINE LTD·07290115934588·

    CONSERVE(R) PLUS CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LZO·August 12, 2024

    K-Wire, Blunt Sharp Tip, L=450, Ø1.7mm XL KWA

    FDA UDI
    PREMIA SPINE LTD·07290115934816·

    CONSERVE(R) HIP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·March 8, 2012

    K-Wire, Blunt Beveled Tip, L=335,Ø 1.7 mm KWA

    FDA UDI
    PREMIA SPINE LTD·07290115935110·

    K-Wire, Blunt Sharp Tip, L=284, Ø1.7mm Short screwdriver+ KWA

    FDA UDI
    PREMIA SPINE LTD·07290115935219·

    ASR 300 SPIKED CUP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·November 19, 2014

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·November 20, 2014

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·April 16, 2013

    ADAPTER SLEEVES 12/14 +5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·November 19, 2014

    ADAPTER SLEEVES 12/14 +2

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·November 4, 2015

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·November 4, 2015

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 15, 2014

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·April 27, 2026

    VARIOUS HIP PROSTHESES SYSTEMS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 5, 2011

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 3, 2021

    PINNACLE SECTOR II CUP 60MM

    FDA Adverse Event
    Injury ·. DEPUY ORTHOPAEDIC INC, 1818910·Product code KWA·May 25, 2018