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510(k) Data Aggregation

    K Number
    K220796
    Date Cleared
    2022-06-10

    (84 days)

    Product Code
    Regulation Number
    870.1220
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The IntellaMap Orion™ High Resolution Mapping Catheter is indicated for electrophysiological mapping (recording or stimulating only) of the cardiac structures of the heart.

    Device Description

    The IntellaMap Orion™ High Resolution Mapping Catheter (Orion catheter) is an 8.5 French (Ø 2.82mm), 115 cm working length, and a 64-electrode steerable catheter. The basket-shaped distal region consists of 8 splines that compose the electrode array. The proximal end has a handle that extends to a cable with a connector. The handle includes bidirectional articulation controls and a deployment slider that activates the electrode array into a basket shape once inside the heart. A flushing port extends from the back of the connector for connection to a continuous pressurized saline drip. The catheter is supplied with an 8.5F insertion sleeve for insertion through the hemostasis valve on an introducer sheath. A sensor in the catheter tip enables the position of the distal region of the catheter to be tracked in space when used with the RHYTHMIA HDx™ Mapping System.

    AI/ML Overview

    This 510(k) summary states that no performance data was applicable for changes proposed in this special 510(k). This is because the new device is substantially equivalent to a previously cleared device, the IntellaMap Orion High-Resolution Mapping Catheter (K192360). The proposed changes were limited to labeling modifications and updated contraindications. Therefore, this document does not contain information about acceptance criteria or a study that proves the device meets specific acceptance criteria.

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