{
  "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": "SAI",
      "openfda": {
        "k_number": [
          "K230088",
          "K242356"
        ],
        "registration_number": [
          "3009189869",
          "3014833750",
          "3011127597",
          "3029890418",
          "3010370500"
        ],
        "fei_number": [
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          "3014833750",
          "3011127597",
          "3029890418",
          "3010370500"
        ]
      },
      "review_panel": "OR",
      "medical_specialty": "OR",
      "device_name": "Ankle Fusion Cage",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Orthopedic",
      "device_class": "2",
      "definition": "Intended for use as an accessory to a tibiotalocalcaneal Intramedullary (IM) rod as part of a fusion construct for failed ankle arthrodesis or failed ankle arthroplasty. Not intended for standalone use.",
      "regulation_number": "888.3020",
      "implant_flag": "Y",
      "submission_type_id": "1"
    }
  ]
}