{
  "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": "2026-10-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "pma_number": "P230017",
      "supplement_number": "S006",
      "applicant": "Medtronic, Inc.",
      "street_1": "8200 Coral Sea St. N.E",
      "street_2": "",
      "city": "Mounds View",
      "state": "MN",
      "zip": "55112",
      "zip_ext": "",
      "generic_name": "Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation",
      "trade_name": "PulseSelect Pulsed Field Ablation (PFA) system",
      "product_code": "QZI",
      "advisory_committee": "CV",
      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "30-Day Notice",
      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2025-05-15",
      "decision_date": "2025-06-13",
      "docket_number": "",
      "decision_code": "OK30",
      "ao_statement": "a change to the sterilization load configuration for devices sterilized at Sterigenics Port Coquitlam",
      "openfda": {
        "registration_number": [
          "3012693387",
          "3017060084",
          "3007029079",
          "3005334138",
          "3008452825",
          "1928237",
          "1721686",
          "3008093809",
          "3011120183",
          "9673241",
          "3001592626",
          "2124215",
          "2182269",
          "3009380063",
          "3000279201",
          "3007603855",
          "3005012805",
          "2183744",
          "1000121056",
          "3008328679",
          "3004593495",
          "3002807314",
          "3007648309",
          "3004859241",
          "3002648230",
          "3009243923",
          "9680579",
          "2024024",
          "3009504230",
          "3012520654",
          "3012263546",
          "3012260771",
          "3004016520",
          "3012179728",
          "3016245399",
          "2182208",
          "1319639",
          "1721983",
          "2184149",
          "9681260",
          "3013300026",
          "2032112",
          "3004105270",
          "3013403214",
          "9612164"
        ],
        "fei_number": [
          "3012693387",
          "3017060084",
          "3007029079",
          "3005334138",
          "3008452825",
          "1000203464",
          "1721686",
          "3008093809",
          "1928237",
          "3011120183",
          "1000138054",
          "3003248396",
          "3001592626",
          "2124215",
          "2182269",
          "3009380063",
          "3000279201",
          "3007603855",
          "3005012805",
          "2183744",
          "1000121056",
          "3008328679",
          "3004593495",
          "3002807314",
          "3003076831",
          "3007648309",
          "3004859241",
          "3002648230",
          "3002806434",
          "3009243923",
          "1000064530",
          "2024024",
          "3009504230",
          "3012520654",
          "3012263546",
          "3012260771",
          "3002806565",
          "1000139754",
          "3004016520",
          "3012179728",
          "3016245399",
          "2182208",
          "3013300026",
          "3004105270",
          "3013403214"
        ],
        "device_name": "Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}