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

    ZENITH PEDICLE SYSTEM

    K Number: K102636 · Decision Mar 3, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    326
    Registration Numbers
    326
    Same Product Code
    308
    Applicant Total
    6
    Review Days
    171

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    Basic Information

    Device Name
    ZENITH PEDICLE SYSTEM
    K Number
    K102636
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Apollo Spine, Inc.
    Date Received
    September 13, 2010
    Decision Date
    March 3, 2011
    Product Code
    MNH
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MNH Orthosis, Spondylolisthesis Spinal Fixation

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    Other Clearances by Apollo Spine, Inc.

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    K090751 COMET ANTERIOR CERVICAL PLATE SYSTEM
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