LogoFDA 510(k) Search
Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K152999
    Device Name
    CorPath 200 System
    Manufacturer
    CORINDUS, INC.
    Date Cleared
    2016-03-18

    (157 days)

    Product Code
    DXX
    Regulation Number
    870.1290
    Type
    Traditional
    Panel
    Cardiovascular
    Reference & Predicate Devices
    K120834,K150892,K111004,K141614
    Why did this record match?
    Reference Devices :

    K120834, K150892, K111004, K141614

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

    The CorPath 200 System is intended for use in the remote delivery and manipulation of guidewires and rapid exchange catheters during percutaneous vascular interventional (PVI) procedures.

    Device Description

    The CorPath 200 System is intended for use by physicians in the delivery and manipulation of guidewires and rapid exchange catheters during percutaneous vascular interventional (PVI) procedures. The CorPath 200 System allows the physician to deliver and manipulate guidewires and catheters through the vasculature under angiography-assisted visual guidance using computer controlled movements while in a seated position and away from the radiation source.

    The CorPath 200 System is composed of two functional sub-units; the Bedside Unit and the Remote Workspace. The Bedside Unit consists of the Articulated Arm, the Robotic Drive and the single-use Cassette. The Remote Workspace consists of the Interventional Cockpit (radiation shield) which houses the Control Console, as well as angiographic monitor(s). Commercially available guidewires and rapid exchange catheters are loaded into the single-use Cassette. By using the joysticks or touch screen of the Control Console, the physician can send commands to the Robotic Drive via a communication cable that advances, retracts or rotates the guidewire, and/or advances or retracts the catheters. The CorPath 200 System's software continuously monitors the communication between the Control Console and the Robotic Drive and alerts the physician if any communication error occurs.

    AI/ML Overview

    Here's an analysis of the provided text, focusing on the acceptance criteria and study data for the CorPath 200 System:

    1. Table of Acceptance Criteria and Reported Device Performance

    The document does not explicitly state acceptance criteria in the form of pre-defined thresholds that the device needed to meet. Instead, it presents the reported performance directly from two clinical studies. However, based on the studies' objectives and reported outcomes, we can infer the implicit "acceptance criteria" related to safety and effectiveness.

    Implicit Acceptance Criteria (Inferred from Study Objectives)Reported Device Performance (PRECISE Study - PCI)Reported Device Performance (RAPID Study - PVI)
    Effectiveness:
    Successful clinical procedural outcome (general)97.6% clinical procedural success100% (29/29) clinical procedural success
    Successful device technical operation98.8% overall device technical success100% (20/20) Device Technical Success (cannulation of target vessel)
    Achievement of treatment goal (e.g., residual stenosis)100% subjects achieved post-procedure stenosis of
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1