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510(k) Data Aggregation

    K Number
    K132363
    Manufacturer
    Date Cleared
    2014-01-16

    (170 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    DOLPHIX EXTERNAL FIXATION SYSTEM

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

    Dolphix® External Fixation System includes various elements designed to build a fixator construct. The system includes fixation bone screws. clamps and rods. Dolphix® External Fixation System is indicated for use in construction of an external fixation frame for treatment of long bone and pelvic fractures that require external fixation. Specifically, the system is intended for:

    • Temporary stabilization of open or closed acute fractures with soft tissue injuries; -
    • Temporary stabilization of fractures in the context of polytrauma: -
    • Temporary stabilization of certain pelvic fractures or pelvic ring injuries; ...
    • Temporary stabilization of limbs after removal of total joint (knee, and ankle) arthroplasty for infection or other failure;
    • Temporary stabilization of non-unions; -
    • Intra-operative temporary stabilization tool to assist with indirect reduction. -

    Dolphix® External Fixation System is intended for use in a non-weight bearing patient.

    Device Description

    Dolphix® External Fixation System includes various elements designed to build a fixator construct. The system includes fixation bone screws. clamps and rods.

    AI/ML Overview

    The provided text is a 510(k) premarket notification letter from the FDA to CITIEFFE s.r.l for their Dolphix® External Fixation System. This document is a regulatory communication concerning the substantial equivalence of a medical device and does not contain any information regarding acceptance criteria, device performance studies, or clinical trial data.

    Therefore, I cannot provide the requested information. The document focuses on regulatory approval based on demonstrating substantial equivalence to a predicate device, not on specific performance data or clinical study results.

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