BEUDAMED
    FDA Registration Active 🇺🇸 United States

    29-FP-5028 Reli™ SP Plus 28mm Female Plate

    Reg #: 3012131184 · FEI: 3012131184 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    CURITEVA, INC.
    Registration Number
    3012131184
    FEI Number
    3012131184
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    25127 WILL MCCOMB DR
    City
    Tanner
    State
    AL
    ZIP
    35671
    Country
    US

    Regulatory Submissions

    510(k) Number
    K151863

    Owner / Operator

    Firm Name
    Curiteva, Inc.
    Operator Number
    10050404
    Address
    25127 Will McComb Drive
    City
    Tanner
    State
    AL
    Postal Code
    35671
    Country
    US
    Correspondent
    Scott L Steelman

    Products

    Device Name Product Code
    Spinous Process Plate PEK

    Proprietary Names

    29-FP-5028 Reli™ SP Plus 28mm Female Plate 29-FP-5055 Reli™ SP Plus 55mm Female Plate 29-FP-5035 Reli™ SP Plus 35mm Female Plate 29-MP-5055 Reli™ SP Plus 55mm Male Plate 29-0128 28mm Trial 29-0145 45mm Trial 29-MP-5035 Reli™ SP Plus 35mm Male Plate 29-MP-5028 Reli™ SP Plus 28mm Male Plate 29-0155 55mm Trial 29-FP-5045 Reli™ SP Plus 45mm Female Plate 29-0135 35mm Trial 29-MP-5045 Reli™ SP Plus 45mm Male Plate

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)