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    FDA 510(k), K152494, Zimmer NexGen Complete Knee Solution Tibial and Femoral Augments

    FDA 510(k), K152494, Zimmer NexGen Complete Knee Solution Tibial and Femoral Augments

    $1,253.22 USD
    $1,253.22 USD
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    510(K) Number: K152494
    Device Name: Zimmer NexGen Complete Knee Solution Tibial and Femoral Augments
    Manufacturer: ZIMMER, INC.
    Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
    Regulation Number: 888.3560
    Classification Product Code: JWH
    Date Received: 09/01/2015
    Decision Date: 11/25/2015
    Regulation Medical Specialty: Orthopedic

    NOTE: 110 of 776 Original Pages Fully Redacted and mostly removed from this file.

    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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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.

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