{
  "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": "2026-08-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Propel Contour Sinus Implant",
        "Propel Sinus Implant",
        "Propel Mini Sinus Implant",
        "Propel Mini Sinus Implant with Straight Deliver System (SDS)"
      ],
      "establishment_type": [
        "Complaint File Establishment per 21 CFR 820.198",
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3008301917",
        "fei_number": "3008301917",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "INTERSECT ENT",
        "address_line_1": "1555 Adams Dr",
        "address_line_2": "",
        "city": "Menlo Park",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "94025",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Medtronic, Inc.",
          "owner_operator_number": "2112641",
          "official_correspondent": {},
          "contact_address": {
            "address_1": "710 Medtronic Parkway",
            "address_2": "",
            "city": "Minneapolis",
            "state_code": "MN",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "55432"
          }
        }
      },
      "pma_number": "P100044",
      "k_number": "",
      "products": [
        {
          "product_code": "OWO",
          "created_date": "2022-11-10",
          "owner_operator_number": "2112641",
          "exempt": "",
          "openfda": {
            "pma_number": [
              "P100044"
            ],
            "device_name": "Drug-Eluting Sinus Stent",
            "medical_specialty_description": "Unknown",
            "regulation_number": "",
            "device_class": "3"
          }
        }
      ]
    }
  ]
}