BEUDAMED
    FDA Registration Active 🇺🇸 United States

    CANNULATED UNI-PLANAR DLTA SCREW

    Reg #: 3010041430 · FEI: 3010041430 · Expires 2025
    View on FDA
    Products
    4
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    4

    Registration Details

    Registration Name
    J&B PRECISION, INC.
    Registration Number
    3010041430
    FEI Number
    3010041430
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    9261 Cordova Park Rd
    City
    Cordova
    State
    TN
    ZIP
    38018
    Country
    US

    Regulatory Submissions

    510(k) Number
    K122571

    Owner / Operator

    Firm Name
    J&B Precision, Inc.
    Operator Number
    10042782
    Address
    9261 Cordova Park Road.
    City
    Cordova
    State
    TN
    Postal Code
    38018
    Country
    US
    Correspondent
    Carl E Buckalew

    Products

    Device Name Product Code
    Thoracolumbosacral Pedicle Screw System NKB
    Orthosis, Spinal Pedicle Fixation MNI
    Appliance, Fixation, Spinal Interlaminal KWP
    Orthosis, Spondylolisthesis Spinal Fixation MNH

    Proprietary Names

    CANNULATED UNI-PLANAR DLTA SCREW

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)