{
  "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": "QRI",
      "openfda": {
        "k_number": [
          "K231141"
        ],
        "registration_number": [
          "3002250546"
        ],
        "fei_number": [
          "3002250546"
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      },
      "review_panel": "NE",
      "medical_specialty": "NE",
      "device_name": "Surgical Planning Software For Neurological Stereotaxic Instruments",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Neurology",
      "device_class": "2",
      "definition": "A surgical planning software for neurological stereotaxic instruments is intended as a stand-alone software device used for pre- and intra-operative planning of stereotactic or image-guided surgeries.",
      "regulation_number": "882.4560",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
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}