BEUDAMED
    FDA Registration Active 🇺🇸 United States

    3911-824-511: KNOTILUS+ 2.4x11.3MM BIOCOMPOSITE, KNOTLESS ANCHOR

    Reg #: 2936485 · FEI: 2936485 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    5
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    STRYKER ENDOSCOPY
    Registration Number
    2936485
    FEI Number
    2936485
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5900 Optical Ct
    City
    SAN JOSE
    State
    CA
    ZIP
    95138
    Country
    US

    Regulatory Submissions

    510(k) Number
    K250544

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Fastener, Fixation, Nondegradable, Soft Tissue MBI
    Fastener, Fixation, Biodegradable, Soft Tissue MAI

    Proprietary Names

    3911-824-511: KNOTILUS+ 2.4x11.3MM BIOCOMPOSITE, KNOTLESS ANCHOR 3911-829-412: KNOTILUS+ 2.9x12.5MM BIOCOMPOSITE, KNOTLESS ANCHOR, HIP 3911-829-512: KNOTILUS+ 2.9x12.5MM BIOCOMPOSITE, KNOTLESS ANCHOR 3911-829-515: KNOTILUS+ 2.9x15.5MM BIOCOMPOSITE, KNOTLESS ANCHOR 3911-824-408: KNOTILUS+ 2.4x8.9MM BIOCOMPOSITE, KNOTLESS ANCHOR, HIP

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device