{
  "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": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Louisville",
      "advisory_committee_description": "Orthopedic",
      "address_1": "357 S. Mccaslin Blvd., Suite 120",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "QLQ",
      "openfda": {
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        "device_name": "Manual Instruments Designed For Use With Total Disc Replacement Devices",
        "medical_specialty_description": "Orthopedic",
        "regulation_number": "888.4515",
        "device_class": "2"
      },
      "zip_code": "80027",
      "applicant": "Synergy Spine Solutions, Inc.",
      "decision_date": "2026-03-27",
      "decision_code": "SESE",
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      "k_number": "K253392",
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      "decision_description": "Substantially Equivalent",
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}