BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    TLIF Curved-P, 32 x 15mm

    DI: M739PP3215 · Model: PP3215 · CAPTIVA SPINE, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    TLIF Curved-P, 32 x 15mm
    Primary DI
    M739PP3215
    Version / Model
    PP3215
    Company Name
    CAPTIVA SPINE, INC.
    Labeler DUNS
    836975784
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2015-08-28
    Public Version
    4
    Public Version Date
    2020-02-24
    Public Version Status
    Update
    Public Device Record Key
    21b15257-32fb-478a-bffd-fac4bf658413
    Distribution End Date
    2017-08-09

    Device Description

    TLIF Curved-P, 32 x 15mm

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    MAX Intervertebral Fusion Device With Bone Graft, Lumbar

    GMDN Terms

    Code Name
    60762 Polymeric spinal interbody fusion cage

    Identifiers

    Type ID
    Primary M739PP3215

    Premarket Submissions

    Submission Number Supplement Number
    K092017 000