BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Solar Lumbar Interbody Fusion System

    Reg #: 3017048829 · FEI: 3017048829 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    LINEAR PRECISION, INC.
    Registration Number
    3017048829
    FEI Number
    3017048829
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1838 A Habersham Square
    City
    Florence
    State
    SC
    ZIP
    29501
    Country
    US

    Regulatory Submissions

    510(k) Number
    K231199

    Owner / Operator

    Firm Name
    Linear Precision, Inc.
    Operator Number
    10075737
    Address
    1838 A Habersham Square
    City
    Florence
    State
    SC
    Postal Code
    29501
    Country
    US
    Correspondent
    Jessica McCracken

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Thoracic PHM
    Intervertebral Fusion Device With Integrated Fixation, Lumbar OVD
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    Solar Lumbar Interbody Fusion System

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)