BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇳 India

    Auxilock Titanium Screw-In Suture Anchor

    K Number: K213104 · Decision Jul 29, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    275
    Registration Numbers
    275
    Same Product Code
    593
    Applicant Total
    12
    Review Days
    308

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    Basic Information

    Device Name
    Auxilock Titanium Screw-In Suture Anchor
    K Number
    K213104
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3040
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Auxein Medical Private Limited
    Date Received
    September 24, 2021
    Decision Date
    July 29, 2022
    Product Code
    MBI
    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
    MBI Fastener, Fixation, Nondegradable, Soft Tissue

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    Other Clearances by Auxein Medical Private Limited

    K Number Device Name
    K221787 Auxein's DHS/DCS Plate System
    K213059 Tibia and Fibula System
    K213110 AUXILOCK PEEK OPTIMA Screw-In Suture Anchor, AUXILOCK ROTADOR PEEK OPTIMA Screw-In Anchor
    K213018 Auxilock GFS Mini, GFS II Large, and GFS Ultimate
    K213108 Humerus & Ulna System
    K213014 Varixis Elbow System
    K213109 Auxilock Draw Tight Suture-Based Anchor
    K211324 2.4mm Distal Radius System
    K210792 Auxein Nailing System
    K203029 Auxilock Titanium Interference Screw
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