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

    ENDIUS SPINE ENDOSCOPE

    K Number: K982819 · Decision Jan 27, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    65
    Registration Numbers
    65
    Same Product Code
    92
    Applicant Total
    33
    Review Days
    169

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    Basic Information

    Device Name
    ENDIUS SPINE ENDOSCOPE
    K Number
    K982819
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1480
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Endius, Inc.
    Date Received
    August 11, 1998
    Decision Date
    January 27, 1999
    Product Code
    GWG
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GWG Endoscope, Neurological

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    Other Clearances by Endius, Inc.

    K Number Device Name
    K080258 MODIFICATION TO ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM
    K073510 ENDIUS TITLE 2 POLY AXIAL SPINAL SYSTEM
    K073267 ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM
    K072840 ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM
    K070282 ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM
    K070367 ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM
    K061345 MODIFICATION TO ENDIUS ATAVI SYSTEM
    K060990 ENDIUS TITLE 2 POLY AXIAL SPINAL SYSTEM
    K060683 ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM
    K053267 ENDIUS ATAVI SYSTEM
    Search all 33 clearances from Endius, Inc. →