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    MODIFICATION TO: ABBOTT VASCULAR SUTURE ANASTOMOSIS DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ABBOTT VASCULAR DEVICES

    FDA Adverse Event
    Malfunction ·PERCLOSE·Product code MGB·January 13, 2003

    ABBOTT VASCULAR DEVICES

    FDA Adverse Event
    Malfunction ·ABBOTT LAB·Product code MGB·September 21, 2004

    ABBOTT VASCULAR DEVICES

    FDA Adverse Event
    Other ·ABBOTT VASCULAR DEVICES·Product code MGB·September 23, 2004

    ABBOTT VASCULAR DEVICES

    FDA Adverse Event
    Injury ·ABBOTT LABORATORIES·Product code MGB·June 20, 2006

    ABBOTT VASCULAR DEVICE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·December 13, 2002

    ABBOTT VASCULAR PROGLIDE PERCLOSE VASCULAR DEVICE

    FDA Adverse Event
    Death ·ABBOTT VASCULAR·Product code MGB·July 31, 2020

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·August 27, 2010

    ABBOTT PROSTAR XL

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·October 25, 2010

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·December 4, 2014

    ABBOTT VASCULAR PERCLOSE DEVICE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·April 10, 2017

    ABBOTT VASCULAR PERCLOSE DEVICE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·April 10, 2017

    ABBOTT VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code MGB·May 22, 2017

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - VASCULAR SOLUTIONS·Product code NIM·October 12, 2009

    ABBOTT PERCLOSE VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·June 22, 2022

    ABBOTT VASCULAR PERCLOSE PROGLIDE VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·November 28, 2022

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·July 13, 2009

    UNKNOWN

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·September 15, 2014

    OMNILINK .035 STENT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code FGE·August 29, 2008

    ABSOLUTE PRO VASCULAR SELF-EXPANDING STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIO·January 21, 2019