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510(k) Data Aggregation

    K Number
    K011447
    Device Name
    IN SPACE 3D
    Date Cleared
    2001-08-03

    (84 days)

    Product Code
    Regulation Number
    892.1750
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K984634

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

    The In Space 3D package is a x-ray imaging software option which allows the reconstruction of two-dimensional images acquired with a standard angiographic C-arm device into a three-dimensional image format.

    The In Space 3D package is intended for imaging both hard and soft tissues as well as other internal body structures(eg. Lesions, Stent implants) for diagnosis, surgical planning, interventional procedures and treatment follow-up.

    As with the FDA cleared 3D Angio software package(K984634), this software package will also assist the physician in diagnosis and treatment of vessel malformations(i.e. Aneurysms, AVMs and Stenoses).

    Device Description

    The In Space 3D package is a x-ray imaging software option which allows the reconstruction of two-dimensional images acquired with a standard angiographic C-arm device into a three-dimensional image format.

    AI/ML Overview

    The provided text is a 510(k) summary for the Siemens In Space 3D Software Option. It describes the device, its intended use, and substantial equivalence to predicate devices, but does not contain information about acceptance criteria or a study that proves the device meets specific performance criteria.

    Therefore, I cannot fulfill the request as the necessary information is not present in the given document. The document focuses on regulatory approval based on substantial equivalence, not on a detailed performance study with acceptance criteria.

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