BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇿🇦 South Africa

    SPICCA Cervical Fusion Cages

    K Number: K230607 · Decision Aug 14, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    339
    Registration Numbers
    339
    Same Product Code
    348
    Applicant Total
    6
    Review Days
    164

    Basic Information

    Device Name
    SPICCA Cervical Fusion Cages
    K Number
    K230607
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    888.3080
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Southern Medical (Pty) , Ltd.
    Date Received
    March 3, 2023
    Decision Date
    August 14, 2023
    Product Code
    ODP
    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
    ODP Intervertebral Fusion Device With Bone Graft, Cervical

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    Other Clearances by Southern Medical (Pty) , Ltd.

    K Number Device Name
    K253373 Southern Craniomaxillofacial (CMF) System
    K230608 SPICCA Stand-Alone Cervical Fusion Cages
    K231145 Axis Anterior Cervical Plate System
    K221182 Southern Transforaminal Lumbar Interbody Fusion (TLIF)
    K221447 Southern Anterior Screw Fixated Cage (SASCA)