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510(k) Data Aggregation

    K Number
    K980763
    Manufacturer
    Date Cleared
    1998-05-28

    (90 days)

    Product Code
    Regulation Number
    878.5040
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    LYSONIX LIPOPLASTY ACCESS PORT

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

    The LySonix Lipoplasty Access Port is indicated for use as an access portal to the surgical site and to reduce trauma to the incision site caused by removal and re-entry of cannulas during lipoplasty procedures during aesthetic body contouring.

    Device Description

    The LySonix Lipoplasty Access Port is an instrument access portal designed for use during lipoplasty procedures for aesthetic body contouring. The device is inserted into the incision site and threaded into place. Once in place, the device threads retain the device in place and allow for the insertion of the lipoplasty cannula. The Lipoplasty Access Portal is designed to be substantially equivalent to Endoscopic Access Devices intended to provide access for surgical instruments and to protect the incision site from trauma during repeated insertion of the cannula during surgical procedures.

    AI/ML Overview

    The provided text does not contain any information about acceptance criteria, device performance studies, sample sizes, expert qualifications, or ground truth establishment.

    The document is an FDA 510(k) clearance letter for the Lysonix Lipoplasty Access Port, indicating that the device is substantially equivalent to a predicate device already on the market. This type of clearance typically relies on demonstrating similarity to an existing device rather than presenting new clinical study data with specific performance metrics and acceptance criteria.

    Therefore, I cannot provide the requested information based on the provided text.

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