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

    GELITA-SPON

    K Number: K051911 · Decision Dec 6, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24
    Same Product Code
    32
    Applicant Total
    2
    Review Days
    145

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    Basic Information

    Device Name
    GELITA-SPON
    K Number
    K051911
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.3620
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Curamedical, BV
    Date Received
    July 14, 2005
    Decision Date
    December 6, 2005
    Product Code
    KHJ
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KHJ Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)

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    Other Clearances by Curamedical, BV

    K Number Device Name
    K060878 GELITA-SPON ABSORBABLE GELATIN SPONGE, USP