BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Altus Spine Titanium Interbody Fusion System

    Reg #: 3009049161 · FEI: 3009049161 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    ALTUS PARTNERS
    Registration Number
    3009049161
    FEI Number
    3009049161
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1340 ENTERPRISE DR
    City
    WEST CHESTER
    State
    PA
    ZIP
    19380
    Country
    US

    Regulatory Submissions

    510(k) Number
    K170512

    Owner / Operator

    Firm Name
    Altus Partners
    Operator Number
    10035934
    Address
    1340 Enterprise Drive
    City
    West Chester
    State
    PA
    Postal Code
    19380
    Country
    US
    Correspondent
    Michael Fitzgerald

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    Altus Spine Titanium Interbody Fusion System

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility