Talar Component, Single Coated/US Version XX-SMALL, LEFT


Product Overview

Talar Component, Single Coated/US Version XX
STAR™ - 400-251


Device Description

A sterile implantable device designed to replace the proximal talus (talar component) as part of a primary ankle joint replacement or prosthesis revision. The device is made of metal [e.g., titanium (Ti), cobalt-chrome (Co-Cr), stainless steel] and is coated with a material (e.g., porous materials, hydroxyapatite) intended to improve fixation and stability by promoting bone ingrowth. Fixation devices for implantation (e.g., screws) may be included and implantation may be performed with or without bone cement.


Environmental Conditions

  • Special Storage Condition, Specify
    • Avoid Exposure to Direct Sunlight or Dampness
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 70.00
    • 50.00
  • Storage Environment Temperature - Degrees Celsius
    • 20.00
    • 18.00

  • Device Sizes

  • LEFT
  • Length: 29 Millimeter
  • Width: 28 Millimeter
    • LEFT
    • Length: 29 Millimeter
    • Width: 28 Millimeter


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: NTG

    Device Name: Prosthesis, Ankle, Uncemented, Non-Constrained

    Device Class: 3

    Physical State: N/A

    Definition: An ankle joint metal/polymer non-constrained uncemented prosthesis is a device intended to be implanted to replace an ankle joint. The device limits minimally (less than normal anatomic constraints) translation in one or more planes. It has no linkage across-the-joint. This generic type of device includes prostheses that have a tibial component made of alloys, such as cobalt-chromium-molybdenum, and a talar component made of ultra-high molecular weight polyethylene.

    Submission Type ID: 2

    Review Panel: OR

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: Y

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Device Identifiers

    Device Id: 00886385016429

    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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