BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    LORENZ ORTHODONTIC ANCHORAGE SYSTEM

    K Number: K063386 · Decision Feb 9, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    54
    Registration Numbers
    54
    Same Product Code
    51
    Applicant Total
    56
    Review Days
    93

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    Basic Information

    Device Name
    LORENZ ORTHODONTIC ANCHORAGE SYSTEM
    K Number
    K063386
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3640
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Walter Lorenz Surgical, Inc.
    Date Received
    November 8, 2006
    Decision Date
    February 9, 2007
    Product Code
    OAT
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OAT Implant, Endosseous, Orthodontic

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    Other Clearances by Walter Lorenz Surgical, Inc.

    K Number Device Name
    K063052 LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATES
    K063506 LORENZ STERNAL CLOSURE SYSTEM
    K062842 TWIST DRILL
    K061384 LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM
    K042516 OTOMIMIX
    K030425 LORENZ RESORBABLE DISTRACTION SYSTEM OR EXPANDER
    K040990 MODIFICATION TO SELF-DRILLING RADIOGRAPHIC MARKERS
    K040983 LORENZ SELF-DRILLING IMF SCREW
    K033740 LORENZ STERNAL CLOSURE SYSTEM
    K032228 LORENZ 2.4 SELF DRILLING SCREWS
    Search all 56 clearances from Walter Lorenz Surgical, Inc. →