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510(k) Data Aggregation

    K Number
    K003045
    Device Name
    HA-TI (HAND TITANIUM SCREW) IMPLANT
    Manufacturer
    HATI DENTAL AG.
    Date Cleared
    2001-07-12

    (286 days)

    Product Code
    DZE
    Regulation Number
    872.3640
    Why did this record match?
    Applicant Name (Manufacturer) :

    HATI DENTAL AG.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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