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    FDA 510(k), K921277, RANAWAT/BURSTEIN TOTAL HIP SYSTEM

    FDA 510(k), K921277, RANAWAT/BURSTEIN TOTAL HIP SYSTEM

    $89.00 USD
    $89.00 USD
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    510(K) Number: K921277
    Device Name: RANAWAT/BURSTEIN TOTAL HIP SYSTEM
    Manufacturer: PATRICIA BERES
    Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
    Regulation Number: LPH
    Classification Product Code: KXA
    Date Received: 03/17/1992
    Decision Date: 02/16/1994
    Decision: Substantially Equivalent (SESE)
    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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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.

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