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

    MODIFIED VERTIFLEX SPINAL SCREW SYSTEM

    K Number: K073143 · Decision Apr 7, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    342
    Registration Numbers
    342
    Same Product Code
    302
    Applicant Total
    5
    Review Days
    152

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    Basic Information

    Device Name
    MODIFIED VERTIFLEX SPINAL SCREW SYSTEM
    K Number
    K073143
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3070
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Vertiflex, Inc.
    Date Received
    November 7, 2007
    Decision Date
    April 7, 2008
    Product Code
    MNI
    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
    MNI Orthosis, Spinal Pedicle Fixation

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    Other Clearances by Vertiflex, Inc.

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    K122509 VERTIFLEX SPINOUS PROCESS FIXATION PLATE
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