BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    Silhouette InstaLift

    K Number: K163676 · Decision Jun 16, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    140
    Registration Numbers
    140
    Same Product Code
    147
    Applicant Total
    5
    Review Days
    171

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    Basic Information

    Device Name
    Silhouette InstaLift
    K Number
    K163676
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4493
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Silhouette Lift, Inc.
    Date Received
    December 27, 2016
    Decision Date
    June 16, 2017
    Product Code
    GAM
    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
    GAM Suture, Absorbable, Synthetic, Polyglycolic Acid

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    Other Clearances by Silhouette Lift, Inc.

    K Number Device Name
    K200140 Silhouette Instalift
    K191299 Silhouette Featherlift / Silhouette Lift
    K171005 Silhouette Featherlift
    K142061 SILHOUETTE INSTALIFT