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510(k) Data Aggregation

    K Number
    K992246
    Date Cleared
    1999-09-03

    (59 days)

    Product Code
    Regulation Number
    892.1170
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    QCT BONE MINERAL ANALYSIS SOFTWARE

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    QCT bone densitometry is indicated for patients with suspected loss of bone to identify QCT bone delistionied I is meetar of the highly responsive spinal trabecular bone is indicated for early detection of bone loss.

    QCT is useful for measuring bone loss or gain with time for monitoring osteoporsis QCT Is useful for mousaning other collect to increased fracture risk by WHO criteria.

    Device Description

    QCT Bone Densitometer (QCT 5000 and QCT 3000)

    AI/ML Overview

    I am sorry, but the provided text from the FDA 510(k) letter and the Indications For Use document does not contain the detailed information necessary to fully answer your request regarding the acceptance criteria and the study that proves the device meets those criteria.

    The documents indicate that the "QCT Bone Mineral Analysis Software" (K992246) and "QCT Bone Densitometer (QCT 5000 and QCT 3000)" were found substantially equivalent to legally marketed predicate devices. However, they do not include the specific performance data, acceptance criteria, study design details, or expert qualifications that your questions ask for.

    To answer your questions, I would need access to the actual 510(k) submission summary or other detailed performance study reports for this device.

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