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

    Streamline OCT Occipito-Cervico-Thoracic System

    K Number: K172139 · Decision Aug 18, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    164
    Registration Numbers
    164
    Same Product Code
    117
    Applicant Total
    9
    Review Days
    32

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    Basic Information

    Device Name
    Streamline OCT Occipito-Cervico-Thoracic System
    K Number
    K172139
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3075
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.)
    Date Received
    July 17, 2017
    Decision Date
    August 18, 2017
    Product Code
    NKG
    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
    NKG Posterior Cervical Screw System

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