1 0

    FDA 510(k), K141405, MOBIS II ST SPINAL IMPLANT

    FDA 510(k), K141405, MOBIS II ST SPINAL IMPLANT

    $89.00 USD
    $89.00 USD
    Sale Sold out
    510(K) Number: K141405
    Device Name: MOBIS II ST SPINAL IMPLANT
    Manufacturer:
    Device Classification Name: Intervertebral Fusion Device With Bone Graft, Lumbar
    Regulation Number: 888.3080
    Classification Product Code: MAX
    Date Received: 05/28/2014
    Decision Date: 09/16/2014
    Regulation Medical Specialty: Orthopedic

    PLEASE NOTE: Most 510(k)s obtained through FOIA are heavily redacted, often omitting sections related to testing, software, manufacturing, and other technical data. Please be sure to review the total pages, redacted pages, and content pages listed in the description to get a sense of how much of the document is redacted. As the FDA FOIA office explains: “We HEAVILY REDACT the majority of the following portions of 510(k) filings: testing data, technical data, lab reports, manufacturing information, vendor information, substantive discussions regarding deficiencies or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.” If you’d like more details about a specific document before purchasing, please contact us at info@foiadocs.com.

    View full details