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

    Baby Gorilla/Gorilla Plating System; Monster Screw System

    K Number: K241262 · Decision Jun 5, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    505
    Registration Numbers
    505
    Same Product Code
    1254
    Applicant Total
    34
    Review Days
    30

    Basic Information

    Device Name
    Baby Gorilla/Gorilla Plating System; Monster Screw System
    K Number
    K241262
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3030
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Paragon 28, Inc.
    Date Received
    May 6, 2024
    Decision Date
    June 5, 2024
    Product Code
    HRS
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HRS Plate, Fixation, Bone

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