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510(k) Data Aggregation

    K Number
    K150640
    Date Cleared
    2015-12-01

    (265 days)

    Product Code
    Regulation Number
    888.3030
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Rx-Fix external fixator is indicated for stabilizing various fractures including open and/or comminuted fractures, infected non-unions, fractures with length discrepancies, fusions and corrective osteotomies. The selection of the appropriate type of fixator is left to the discretion of the type of fracture and patient's and patient's anatomy.

    Device Description

    The subject RX-FIX Minirail External Fixator is a stable solution for fractures and for lengthening of small bones. It is used for comminuted intra-articular fractures, joint stiffness, or arthrodesis of the foot or hand. The RX-FIX allows for variable pin placement in transverse and frontal planes to simplify external fixation applications on several surgical procedures including: fusions, corrective osteotomies, and fracture fixation. The pin clamp allows for both compression and distraction of the pins.

    AI/ML Overview

    This document is a 510(k) premarket notification for the RX-FIX Mini Rail External Fixator. It focuses on demonstrating substantial equivalence to a predicate device based on technological characteristics, rather than presenting a study to prove a device meets specific acceptance criteria based on performance metrics such as sensitivity, specificity, or F1 score.

    Therefore, the requested information regarding acceptance criteria, device performance tables, sample sizes for test/training sets, expert involvement, and ground truth establishment is not available in the provided text, as these are typically associated with performance studies for software devices or diagnostics.

    The document explicitly states:

    • (b)(1). Substantial Equivalence Non-Clinical Evidence N/A
    • (b)(2). Substantial Equivalence Clinical Evidence N/A

    This indicates that no dedicated performance study (clinical or non-clinical) was conducted or presented to the FDA for this 510(k) submission, as the determination of substantial equivalence was based on technological characteristics and intended use being similar to a legally marketed predicate device (K051017: R-X-FIX Eternal Fixator).

    Thus, I cannot provide the requested information.

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