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

    ChoiceSpine TigerShark™ M, Modular Interbody System

    K Number: K220953 · Decision Sep 13, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    418
    Registration Numbers
    418
    Same Product Code
    890
    Applicant Total
    9
    Review Days
    165

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    Basic Information

    Device Name
    ChoiceSpine TigerShark™ M, Modular Interbody System
    K Number
    K220953
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3080
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Choice Spine, LLC
    Date Received
    April 1, 2022
    Decision Date
    September 13, 2022
    Product Code
    MAX
    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
    MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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    Other Clearances by Choice Spine, LLC

    K Number Device Name
    K223869 ChoiceSpine Blackhawk Ti Cervical Spacer System
    K220024 ChoiceSpine Navigation System
    K211449 Triton™ Sacroiliac Joint Fixation System
    K203311 ChoiceSpine Blackhawk Ti Cervical Spacer System
    K203561 ChoiceSpine Navigation System
    K201643 ChoiceSpine Tiger Shark Cervical Spacer System
    K191621 ChoiceSpine Octane A/T/P Spinal Implant System, ChoiceSpine Cervical Interbody Spacer System Ascendant PC, ChoiceSpine Cervical Interbody Spacer System Ascendant, ChoiceSpine Cervical Spacer System Blackhawk, ChoiceSpine Intervertebral Fusion Device Octane Straight, ChoiceSpine Intervertebral Fusion Device Octane Straight PC, ChoiceSpine VEO Laterial Access & Interbody Fusion System
    K191367 Harrier-SA Lumbar Interbody System