{
  "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": "2026-06-01",
    "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": "OQB",
      "openfda": {
        "k_number": [
          "DEN200010",
          "K230927",
          "K231781",
          "K251302"
        ],
        "registration_number": [
          "2135156",
          "1450662"
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        "fei_number": [
          "3003179719",
          "1450662"
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      },
      "review_panel": "OR",
      "medical_specialty": "OR",
      "device_name": "Intervertebral Body Graft Containment Device",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Orthopedic",
      "device_class": "2",
      "definition": "An intervertebral body graft containment device is a non-rigid, implanted spinal device that is designed to contain bone graft within its internal cavity. The device is inserted into the intervertebral body space of the spine and is intended as an adjunct to intervertebral body fusion.",
      "regulation_number": "888.3085",
      "implant_flag": "Y",
      "submission_type_id": "1"
    }
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}