{
  "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": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QNI",
      "openfda": {
        "k_number": [
          "K243578",
          "K251214",
          "DEN200035"
        ],
        "registration_number": [
          "2530154",
          "3013820501",
          "3020652309"
        ],
        "fei_number": [
          "3013820501",
          "3020652309",
          "1000307073"
        ]
      },
      "review_panel": "OR",
      "medical_specialty": "OR",
      "device_name": "Resorbable Implant For Anterior Cruciate Ligament (Acl) Repair",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Orthopedic",
      "device_class": "2",
      "definition": "A resorbable implant for anterior cruciate ligament (ACL) repair is a degradable material that allows for healing of a torn ACL that is biomechanically stabilized by traditional suturing procedures. The device is intended to protect the biological healing process from the surrounding intraarticular environment and not intended to replace biomechanical fixation via suturing. This classification includes devices that bridge or surround the torn ends of a ruptured ACL.",
      "regulation_number": "888.3044",
      "implant_flag": "Y",
      "submission_type_id": "1"
    }
  ]
}