{
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    "terms": "https://open.fda.gov/terms/",
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      "supplement_number": "S009",
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      "street_1": "7555 Innovation Way",
      "street_2": "",
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      "generic_name": "Surgical cardiac ablation device, for treatment of atrial fibrillation",
      "trade_name": "Cannula with Guide",
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      "advisory_committee": "CV",
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      "supplement_type": "Normal 180 Day Track",
      "supplement_reason": "Labeling Change - Indications/instructions/shelf life/tradename",
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      "date_received": "2024-05-31",
      "decision_date": "2024-08-28",
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      "decision_code": "APPR",
      "ao_statement": "an alternate pigment for the Cannula with Guide (CSK-6131)",
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