{
  "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": "2026-07-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QML",
      "openfda": {
        "k_number": [
          "DEN240007"
        ],
        "registration_number": [
          "3015615781",
          "3038193698",
          "3008889904"
        ],
        "fei_number": [
          "3015615781",
          "3038193698",
          "3008889904"
        ]
      },
      "review_panel": "SU",
      "medical_specialty": "SU",
      "device_name": "Anal Fistula Closure Device",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General, Plastic Surgery",
      "device_class": "2",
      "definition": "An anal fistula closure device is a surgical implant for anal fistula repair and is intended for closure of the anal fistula.  The device may be manually applied or delivered with a delivery device.",
      "regulation_number": "878.4835",
      "implant_flag": "Y",
      "submission_type_id": "1"
    }
  ]
}