Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K960643
    Manufacturer
    Date Cleared
    1996-12-16

    (306 days)

    Product Code
    Regulation Number
    888.3390
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Single use, camented or pressfit hip replacement component for use in patients requiring joint replacement due to trauma, disease or failed previous hip replacement surgery.

    Device Description

    The Achantage MAPF Femoral Component is a cobalt alloy (Co-Cr-Mo) fernoral stam which is designed to articulate with any commercially available acetabular component. It has no linkage across the joint.

    The MAPF devices are straight, as apposed to anatomic or curved in design. This eliminates the need for left and right configurations thus recucing the cost of inventory to the hospital. The Hosam distal goometry increases the strength and flexibility of the device. The lateral edge of the device is straight which anables the surgeon to rasp and asat the prosthesis, without creating a gap in the proximal lateral aspect of the femur. A lateral fin provides rotational stability. The duckbill type collar prevents subsidence.

    Available in 6 sizes (diameters) for easier patient matching, all sizes are 160mm in length with a neck length of 32mm. Because this device is usually used in the older, low demand patient, it would most often be used in conjunction with a bipolar or endoprosthetic head.

    AI/ML Overview

    This document is a Summary of Safety and Effectiveness for a medical device, specifically a hip femoral component. It does not describe an AI/ML-enabled device or a study to prove acceptance criteria for such a device.

    The document focuses on the physical characteristics, indications for use, potential risks, and substantial equivalence of a traditional medical implant. Therefore, I cannot extract the requested information (acceptance criteria, device performance, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth types, or training set details) as they pertain to the evaluation of an AI/ML system.

    The provided text is a pre-market submission for a conventional medical device, not a study evaluating an algorithmic product.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1