BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HYPROCURE

    MDR report key: 11852017 · Received May 19, 2021

    Report

    Report Number
    3004993707-2021-00009
    Event Type
    Injury
    Date Received
    May 19, 2021
    Date of Event
    August 8, 2019
    Report Date
    April 12, 2021
    Manufacturer
    GRAHAM MEDICAL TECHNOLOGIES, LLC. DBA GRAMEDICA
    Product Code
    HWC
    UDI-DI
    M621HYP070
    PMA / PMN Number
    K042030
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A MULTICENTER POST MARKET CLINICAL FOLLOW-UP RETROSPECTIVE STUDY IS BEING PERFORMED AT SPECIFIC TIME POINTS POST-IMPLANTATION TO EVALUATE THE SAFETY AND PERFORMANCE OF THE HYPROCURE IMPLANT. THE PMCF STUDIES WERE NOT REQUESTED BY FDA. NO COMPLAINTS HAVE BEEN MADE TO THE MANUFACTURER. PATIENT DID NOT RECEIVE ADEQUATE CORRECTION OF FOOT ALIGNMENT. NO REASONS WERE PROVIDED. POSSIBLY NOT A GOOD CANDIDATE FOR PROCEDURE. NO OTHER INFORMATION WAS GIVEN.

    Description of Event or Problem · 1

    THE DEVICE DID NOT IMPROVE MY FOOT ALIGNMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    746728 HYPROCURE HYPROCURE SUBTALAR IMPLANT HWC GRAHAM MEDICAL TECHNOLOGIES, LLC. DBA GRAMEDICA HYP-07 070206171 M621HYP070

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Other