BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    NA

    DI: 10885862527240 · Model: 02-521-20-2000 · Exactech, Inc.
    View on AccessGUDID
    Product Codes
    2
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    NA
    Primary DI
    10885862527240
    Version / Model
    02-521-20-2000
    Catalog Number
    02-521-20-2000
    Company Name
    Exactech, Inc.
    Labeler DUNS
    157565946
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-07-28
    Public Version
    1
    Public Version Date
    2022-08-05
    Public Version Status
    New
    Public Device Record Key
    454fd19f-029d-4a1f-82ec-29d752b766ea

    Device Description

    TKA PLUS TIBIAL RESECTION GUIDE RIGHT

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    HAW Neurological stereotaxic Instrument
    OLO Orthopedic stereotaxic instrument

    GMDN Terms

    Code Name
    45200 Orthopaedic stereotactic surgery system

    Identifiers

    Type ID
    Primary 10885862527240

    Premarket Submissions

    Submission Number Supplement Number
    K100742 000
    K152764 000
    K193618 000