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510(k) Data Aggregation

    K Number
    K060403
    Manufacturer
    Date Cleared
    2006-03-28

    (41 days)

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

    PTA (PROGRESSIVE TIBIAL ALIGNMENT)

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

    The PTA (Progressive Tibial Alignment) external fixation system is a modular system with the components of: joints, bars, clamps or screws. Such components form a device indicated for reconstruction and corrections of bone segments of the human body.

    The PTA is for progressive realignment of the knee.

    Device Description

    The PTA has multiple components of metallic bone fixation appliances and accessories. It is designed for a progressive correction of the lower limb using tibial osteotomy. This device is composed of a main section of a bar and proximal distraction unit upon which are connected the clamps and grasping components. All components are made of either Aluminum alloy 7012 or Stainless steel, AISI 316 LVM, ISO 5832-1.

    AI/ML Overview

    The provided text is a 510(k) Summary for the PTA (Progressive Tibial Alignment) external fixation system. This document is for a medical device that realigns bone segments, primarily for progressive realignment of the knee, and it's seeking clearance based on substantial equivalence to a predicate device (FEP, K032427).

    Crucially, the provided text DOES NOT contain the type of information requested about acceptance criteria, study details, performance metrics, ground truth establishment, or sample sizes related to an AI/algorithm-based device.

    The document describes a physical medical device (an external fixation system) and its components, materials, and intended use. It focuses on demonstrating substantial equivalence to a previously cleared device, not on evaluating the performance of a software algorithm.

    Therefore, I cannot extract the requested information. The prompt specifically asks for details related to acceptance criteria and a study proving device meets these criteria, typically found in submissions for AI/ML-driven devices or diagnostic tools. This document is for a mechanical orthopedic device.

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