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

    STALIF TT

    K Number: K051027 · Decision Jun 29, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    222
    Registration Numbers
    222
    Same Product Code
    276
    Applicant Total
    10
    Review Days
    68

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    Basic Information

    Device Name
    STALIF TT
    K Number
    K051027
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3060
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Surgicraft , Ltd.
    Date Received
    April 22, 2005
    Decision Date
    June 29, 2005
    Product Code
    MQP
    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
    MQP Spinal Vertebral Body Replacement Device

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    Other Clearances by Surgicraft , Ltd.

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    K041617 STALIF TT
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    K965221 RANSFORD CERVICAL FIXATION SYSTEM