{
  "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": "2026-07-27",
    "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": "QVV",
      "openfda": {
        "k_number": [
          "DEN220033"
        ],
        "registration_number": [
          "3008274656",
          "2953359",
          "2029275"
        ],
        "fei_number": [
          "3008274656",
          "3000215205",
          "1000306431"
        ]
      },
      "review_panel": "OR",
      "medical_specialty": "OR",
      "device_name": "Medial Knee Implanted Shock Absorber",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Orthopedic",
      "device_class": "2",
      "definition": "A medial knee implanted shock absorber is a device implanted outside of the knee capsule extending from the distal femur to the proximal tibia. It is intended to reduce loads on the intra-articular medial joint surface. The device employs a shock absorbing mechanical system and is biomechanically stabilized by plates and screws. The device is not intended to span the lateral knee.",
      "regulation_number": "888.3610",
      "implant_flag": "Y",
      "submission_type_id": "1"
    }
  ]
}