{
  "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",
    "results": {
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  "results": [
    {
      "pma_number": "P240003",
      "supplement_number": "",
      "applicant": "Renata Medical, Inc.",
      "street_1": "4695 Macarthur Ct.",
      "street_2": "Suite 440",
      "city": "Newport Beach",
      "state": "CA",
      "zip": "92660",
      "zip_ext": "",
      "generic_name": "Aortic stent",
      "trade_name": "Minima Stent System",
      "product_code": "PNF",
      "advisory_committee": "CV",
      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "",
      "supplement_reason": "",
      "expedited_review_flag": "N",
      "date_received": "2024-03-01",
      "decision_date": "2024-08-28",
      "docket_number": "",
      "decision_code": "APPR",
      "ao_statement": "The Minima Stent System is indicated for use in the treatment of native or acquired pulmonary artery stenoses or coarctation of the aorta in neonates, infants, and children at least 1.5 kg in weight.",
      "openfda": {
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        "device_name": "Aortic Stent",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
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}