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510(k) Data Aggregation

    K Number
    K961959
    Date Cleared
    1996-07-19

    (60 days)

    Product Code
    Regulation Number
    878.4800
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K944837

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

    The MD Tech Biopsy-Set is intended for the purpose of harvesting bone and/or bone marrow specimens.

    Device Description

    Our company is presently authorized by the Food and Drug Administration to manufacture soft tissue biopsy needles, K944837 The bone biopsy needle is a variation of this needle.

    The MD Tech Biopsy-Set Bone and Bone marrow is inserted percutaneously, adjacent to the biopsy site. Access to the bone and/or bone marrow specimen(s) is achieved mechanically via cutting surfaces on the device. Harvesting of bone and/or bone marrow specimen(s) is accomplished both by mechanical and negative pressure (aspiration), which is created by attaching a syringe to a fitting on the outer cannula of the device. Specimen(s) are contained within the outer cannula during withdrawal from the patient.

    AI/ML Overview

    The provided text does not contain information about acceptance criteria, device performance metrics, or any study details that would allow for the completion of the requested table and subsequent questions. The document is a 510(k) summary for a bone and bone marrow biopsy needle, focusing on substantial equivalence to predicate devices and a description of the device's intended use and mechanism. It does not include data from performance studies.

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