{
  "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": "2026-11-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "Y",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "OBA",
      "openfda": {
        "registration_number": [
          "2011171",
          "1721676"
        ],
        "fei_number": [
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          "1721676"
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      },
      "review_panel": "NE",
      "medical_specialty": "",
      "device_name": "Polymerizing, Neurovascular Embolization Material",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Unknown",
      "device_class": "f",
      "definition": "The neurovascular embolization device is placed in a blood vessel to permanenty obstruct blood flow to an intracranial aneurysm or other vascular malformation.   The device polymerizes or precipitates in situ.",
      "regulation_number": "",
      "implant_flag": "Y",
      "submission_type_id": "6"
    }
  ]
}