{
  "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": "2026-11-02",
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      "applicant": "Nuvectra Corporation",
      "street_1": "10675 Naples St. NE",
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      "city": "Blaine",
      "state": "MN",
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      "generic_name": "Stimulator, spinal-cord, totally implanted for pain relief",
      "trade_name": "Algovita Spinal Cord Stimulation System",
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      "advisory_committee_description": "Neurology",
      "supplement_type": "30-Day Notice",
      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2019-07-29",
      "decision_date": "2019-08-28",
      "docket_number": "",
      "decision_code": "OK30",
      "ao_statement": "Implementation of an update to the injection molding process for the distal subassembly of the Algovita® 12-Electrode Percutaneous Leads, Trial Leads, and LeadExtensions.",
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