Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K041810
    Manufacturer
    Date Cleared
    2004-12-21

    (168 days)

    Product Code
    Regulation Number
    878.4400
    Why did this record match?
    Device Name :

    SERFAS ENERGY SYSTEM

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

    The SERFAS Energy System is indicated for resection ablation and coagulation of soft tissue and hemostasis of blood vessels in orthopedic and arthroscopic procedures of joints such as the knee, shoulder, elbow, hip, ankle and wrist.

    Device Description

    The SERFAS Energy System is a bipolar high frequency electrosurgical system comprised of an electrosurgical generator, a series of disposable, single use, probe styles, and a footswitch.

    AI/ML Overview

    I am sorry, but the provided text does not contain the information required to answer your request. The document is a 510(k) summary for the SERFAS Energy System, which describes its intended use, predicate devices, and concludes with an assessment of substantial equivalence.

    It does not include details on:

    1. Acceptance criteria and reported device performance.
    2. Sample sizes, data provenance, or details about test sets.
    3. Number and qualifications of experts, or ground truth establishment methods.
    4. Adjudication methods.
    5. Multi-reader multi-case (MRMC) comparative effectiveness studies.
    6. Standalone algorithm performance.
    7. Types of ground truth used.
    8. Training set sample size or how its ground truth was established.

    This document focuses on regulatory clearance based on substantial equivalence to predicate devices, rather than a detailed presentation of performance study results against specific acceptance criteria.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1