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

    MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT

    K Number: K062004 · Decision Aug 15, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    222
    Registration Numbers
    222
    Same Product Code
    276
    Applicant Total
    5
    Review Days
    29

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    Basic Information

    Device Name
    MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT
    K Number
    K062004
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    888.3060
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Quantum Orthopedics, Inc.
    Date Received
    July 17, 2006
    Decision Date
    August 15, 2006
    Product Code
    MQP
    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
    MQP Spinal Vertebral Body Replacement Device

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    Other Clearances by Quantum Orthopedics, Inc.

    K Number Device Name
    K061576 MODIFICATION TO QUANTUM VERTEBRAL BODY REPLACEMENT SYSTEM
    K052641 MODIFICATION TO: QUANTUM VERTEBRAL BODY REPLACEMENT
    K060491 QUANTUM ANTERIOR CERVICAL PLATE SYSTEM
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