{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-20",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Pleasanton",
      "advisory_committee_description": "Gastroenterology, Urology",
      "address_1": "4155 Hopyard Rd.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "PEW",
      "openfda": {
        "device_name": "Implantable Transprostatic Tissue Retractor System",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5530",
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      "applicant": "Neotract, Inc.",
      "decision_date": "2020-07-31",
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      "country_code": "US",
      "device_name": "UroLift 2 System (formerly UL500), UroLift 2 Delivery Handle, UroLift 2 Implant Cartridge",
      "advisory_committee": "GU",
      "contact": "Brian  Gall",
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      "k_number": "K201837",
      "state": "CA",
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      "decision_description": "Substantially Equivalent",
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