{
  "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": "2026-08-17",
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      "pma_number": "P210007",
      "supplement_number": "S004",
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      "street_1": "2802 Flintrock Trace, Suite 226",
      "street_2": "",
      "city": "Austin",
      "state": "TX",
      "zip": "78738",
      "zip_ext": "",
      "generic_name": "Stimulator, autonomic nerve, implanted for stroke rehabilitation",
      "trade_name": "MicroTransponder® Vivistim® Paired VNS™ System",
      "product_code": "QPY",
      "advisory_committee": "PM",
      "advisory_committee_description": "Physical Medicine",
      "supplement_type": "30-Day Notice",
      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2025-01-15",
      "decision_date": "2025-01-24",
      "docket_number": "",
      "decision_code": "OK30",
      "ao_statement": "undefined",
      "openfda": {
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        "medical_specialty_description": "Unknown",
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