{
  "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/",
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    "last_updated": "2026-10-12",
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      "supplement_number": "S003",
      "applicant": "AtriCure, Inc.",
      "street_1": "7555 Innovation Way",
      "street_2": "",
      "city": "Mason",
      "state": "OH",
      "zip": "45040",
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      "generic_name": "Surgical cardiac ablation device, for treatment of atrial fibrillation",
      "trade_name": "EPi-Sense® Guided Coagulation System and EPi-Sense ST™ Coagulation System",
      "product_code": "OCM",
      "advisory_committee": "CV",
      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "Normal 180 Day Track No User Fee",
      "supplement_reason": "Postapproval Study Protocol",
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      "date_received": "2022-09-13",
      "decision_date": "2022-10-13",
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      "decision_code": "APPR",
      "ao_statement": "Approval of the revised protocol for the post-approval study (PAS) protocol.",
      "openfda": {
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