BONE TUNNEL PLUGS CANN 7-12MM LTX


Product Overview

BONE TUNNEL PLUGS CANN 7
NA - 7210149


Device Description

A sterile device intended to be inserted into a bone tunnel during an arthroscopic procedure to reduce the loss of the irrigation fluid used to maintain visualization, while allowing the passage of instruments (e.g., probes, guide pins, shavers and graspers) through its lumen to access the joint. It is a short, rigid, cannulated tube which tapers distally with a penetrable seal on the proximal end. It is inserted manually into the bone tunnel, or may be supplied with dedicated instruments for insertion (e.g., obturator). The device is available in a variety of diameters, and is typically made of plastic. This is a single-use device.


Environmental Conditions

  • Special Storage Condition, Specify
    • 0

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: HRX

    Device Name: Arthroscope

    Device Class: 2

    Physical State: N/A

    Definition: Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

    Submission Type ID: 1

    Review Panel: OR

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 888.1100

    Third Party Flag: Y

    Medical Specialty: OR


    Device Identifiers

    Device Id: 23596010495918

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 03596010495914

    Package Quantity: 6

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: BX


    Device Id: 03596010495914

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


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