BEUDAMED
    FDA Registration Active 🇺🇸 United States

    RESPONSIVE ARTHROSCOPY

    Reg #: 3015200759 · FEI: 3015200759 · Expires 2026
    View on FDA
    Products
    6
    Proprietary Names
    25
    Establishment Types
    1
    Classifications
    6

    Registration Details

    Registration Name
    RESPONSIVE ARTHROSCOPY
    Registration Number
    3015200759
    FEI Number
    3015200759
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    701 N 3rd Street, Suite 208
    City
    Minneapolis
    State
    MN
    ZIP
    55401
    Country
    US

    Regulatory Submissions

    510(k) Number
    K202153

    Owner / Operator

    Firm Name
    Responsive Arthroscopy
    Operator Number
    10059367
    Address
    701 N 3rd Street, Suite 208
    City
    Minneapolis
    State
    MN
    Postal Code
    55401
    Country
    US
    Correspondent
    Gretchen Hinchley

    Products

    Device Name Product Code
    Fastener, Fixation, Nondegradable, Soft Tissue MBI
    Tray, Surgical, Instrument FSM
    Screw, Fixation, Bone HWC
    Orthopedic Manual Surgical Instrument LXH
    Staple, Fixation, Bone JDR
    Bit, Surgical GFG

    Proprietary Names

    Superhawk Instruments-Spirit, Hornet, Lightning, Nighthawk, Superhawk, Mini Superhawk, Thunderbolt, Mini Stealth, Stealth, Shadow Stealth and Mini Stealth All-Suture Anchors, Shadow and Shadow Mini All-Suture Anchors Shadow Knotless All-Suture Anchors Nighthawk Suture Anchor Osprey Suture Anchor Falcon Spirit Mustang and Mustang Knotless Vented Suture Anchors Eagle and Eagle Knotless Suture Anchors Agile Instruments Thunderbolt Eagle Lightning Stealth Shadow Shadow Knotless Shadow Mini Lightning Suture Anchor Hornet Suture Anchor Valor Suture Anchor Super Hornet Mustang Knotless Agile Suture Anchor Mini Superhawk Suture Anchor

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility