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510(k) Data Aggregation

    K Number
    K172501
    Date Cleared
    2017-09-21

    (34 days)

    Product Code
    Regulation Number
    888.3358
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The iNSitu Total Hip System is indicated for use in skeletally mature individuals undergoing surgery for total hip replacement due to:

    · A severely painful and or disabled joint from osteoarthritis, traumator arthritis, avascular necrosis, or congenital hip dysplasia;

    · Acute traumatic fracture of the femoral head or neck;

    · Failed previous hip surgery including joint reconstruction, arthrodesis, hemiarthroplasty, surface replacement arthroplasty or total hip replacement

    The iNSitu Total Hip System femoral stem is intended for cementless fixation. The iNSitu Total Hip System acetabular cup is intended for cementless fixation. The porous structured surfaces provide biological fixation in a cementless application.

    Device Description

    The iNSitu Total Hip Replacement System is an artificial total hip replacement system includes femoral stems manufactured from forged Ti 6Al-4V ELI material, femoral heads manufactured from CoCr alloy and BIOLOX® delta ceramic, acetabular cups (additively manufactured from Ti), acetabular liners manufactured from Vitamin E polyethylene, acetabular bone screws, screw hole covers for the screw holes in the acetabular cups, and apical hole covers for the apical hole in the acetabular cups manufactured from Ti 6Al-4V ELI material.

    AI/ML Overview

    The provided text is a 510(k) summary for the iNSitu Total Hip System, a medical device for total hip replacement. It demonstrates substantial equivalence to a predicate device and includes information about performance testing.

    However, the provided document does not contain information about a study proving that an AI/device meets acceptance criteria, or any of the detailed information requested in the prompt regarding AI model performance, ground truth establishment, sample sizes for training/test sets, expert adjudication, or MRMC studies.

    Therefore, I cannot extract the requested information from the provided text. The document describes a physical medical device (hip replacement system) and its performance testing as per FDA regulations for 510(k) clearances, which typically involves mechanical and material properties, not AI algorithm performance.

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