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    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

    PERMATAPE

    K Number: K162247 · Decision Dec 15, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    242
    Registration Numbers
    242
    Same Product Code
    173
    Applicant Total
    96
    Review Days
    127

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    Basic Information

    Device Name
    PERMATAPE
    K Number
    K162247
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.5000
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medos International SARL
    Date Received
    August 10, 2016
    Decision Date
    December 15, 2016
    Product Code
    GAT
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GAT Suture, Nonabsorbable, Synthetic, Polyethylene

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