REDAPT ANTEVERTED CEMENTED XLPE ACETABULAR LINER 40MM X 76-80MM


Product Overview

REDAPT ANTEVERTED CEMENTED XLPE ACETABULAR LINER 40MM X 76
REDAPT - 71354271


Device Description

A sterile, implantable component of a two-piece acetabulum prosthesis that is inserted into an acetabular shell prosthesis to provide the articulating surface with a femoral head prosthesis as part of a total hip arthroplasty (THA). It is made of polyethylene (includes hylamer, cross-linked polyethylene), and does not include a stabilizing component to limit the range of motion of the hip.


Environmental Conditions

No Data Available


Device Sizes

  • 40MM OD 76-80MM ID: 76-80 Millimeter
    • 40MM OD 76-80MM ID: 76-80 Millimeter


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: JDI

    Device Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    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: Y

    Target Area: N/A

    Regulation Number: 888.3350

    Third Party Flag: N

    Medical Specialty: OR


    Code: KWZ

    Device Name: Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    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: Y

    Target Area: N/A

    Regulation Number: 888.3310

    Third Party Flag: N

    Medical Specialty: OR


    Code: LZO

    Device Name: Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    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: Y

    Target Area: N/A

    Regulation Number: 888.3353

    Third Party Flag: N

    Medical Specialty: OR


    Device Identifiers

    Device Id: 00885556322994

    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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