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510(k) Data Aggregation

    K Number
    K981156
    Date Cleared
    1998-05-20

    (50 days)

    Product Code
    Regulation Number
    888.1100
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    DYONICS INTELIJET INFLOW/OUTFLOW CANNULA

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

    The Dyonics® InteliJET™ Inflow/Outflow Cannula is indicated for use with the InteliJET Fluid Management System during arthroscopic surgical procedures of the knee, shoulder and small joints to regulate flow of irrigation fluids through the joint to maintain intra-articular pressure for uniform distention and clear visualization of the surgical site.

    Device Description

    The Dyonics InteliJET Inflow/Outflow Cannula is used to establish a portal to the surgical site during arthroscopic surgical procedures. The Dyonics InteliJET Inflow/Outflow Cannula is designed to work in conjunction with the InteliJET Fluid Management System to maintain intraarticular pressure for uniform distention and clear visualization of the surgical site.

    AI/ML Overview

    This 510(k) summary describes a device, the Dyonics® InteliJET™ Inflow/Outflow Cannula, which is a hardware component. The provided text does not include any information about an AI/ML powered device, a study designed to prove the device meets acceptance criteria, or acceptance criteria itself. The document focuses on establishing substantial equivalence to predicate devices based on design, materials, principle of operation, and intended use for regulatory clearance. It does not contain the type of performance evaluation details requested for AI/ML devices. Therefore, I cannot generate the requested table and answer the study-related questions.

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