BEUDAMED
    FDA Registration Active 🇺🇸 United States

    N8TIVE ACL Trans Tibial Center Guide

    Reg #: 3006524618 · FEI: 3010813691 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    7
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ArthroCare Corporation
    Registration Number
    3006524618
    FEI Number
    3010813691
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7000 W William Cannon Dr
    City
    Austin
    State
    TX
    ZIP
    78735
    Country
    US

    Owner / Operator

    Firm Name
    Smith & Nephew, Inc.
    Operator Number
    1020279
    Address
    2875 Railroad Street
    City
    Pittsburgh
    State
    PA
    Postal Code
    15222
    Country
    US
    Correspondent
    Lisa Ewing

    Products

    Device Name Product Code
    Brace, Drill HXY

    Proprietary Names

    N8TIVE ACL Trans Tibial Center Guide SpeedLock HIP Drill Guide HipSlide Slotted Cannula Insertion Guide N8TIVE ACL Femoral Drill Guide N8TIVE ACL Femoral Pin Guide N8TIVE ACL Tibial Pin Guide N8TIVE ACL Femoral Footprint Template

    Establishment Types

    Repack or Relabel Medical Device