BEUDAMED
    FDA Registration Active 🇺🇸 United States

    InterV Curette; InterV Direct Access Needle

    Reg #: 3008583793 · FEI: 3008583793 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    9
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    ZAVATION
    Registration Number
    3008583793
    FEI Number
    3008583793
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3670 Flowood Dr
    City
    Flowood
    State
    MS
    ZIP
    39232
    Country
    US

    Owner / Operator

    Firm Name
    Zavation Medical Products LLC
    Operator Number
    10055475
    Address
    3670 Flowood Dr
    City
    Flowood
    State
    MS
    Postal Code
    39232
    Country
    US
    Correspondent
    Elke Carter

    Products

    Device Name Product Code
    Spinal Channeling Instrument, Vertebroplasty OCJ

    Proprietary Names

    InterV Curette; InterV Direct Access Needle Blue Diamond Digital Inflation Vertebrex Bone Access Needle; Vertebrex Curette; InterV Kirschner Wire; Vertebrex Bone Access Cannula; InterV Bone Access Cannula; InterV Bone Access Needle; InterV Drill; InterV Flex Needle; Vertebrex Direct Access Needle; Vertebrex Drill; Vertebrex Flex Needle Atrion QL2530 Inflation Device Vertebrex Kirschner Wire; ZV Plasty Direct Access Needle

    Establishment Types

    Repack or Relabel Medical Device Complaint File Establishment per 21 CFR 820.198