{
  "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": "2026-05-25",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Cordova",
      "advisory_committee_description": "General, Plastic Surgery",
      "address_1": "51 Germantown Ct.",
      "address_2": "Suite 200",
      "statement_or_summary": "Summary",
      "product_code": "QUW",
      "openfda": {
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        "device_class": "2",
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      "applicant": "Theramicro",
      "decision_date": "2025-05-30",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "TekBrace Solo Soft Tissue Reinforcement Device",
      "advisory_committee": "SU",
      "contact": "Christine  Scifert",
      "expedited_review_flag": "",
      "k_number": "K251063",
      "state": "TN",
      "date_received": "2025-04-04",
      "review_advisory_committee": "OR",
      "postal_code": "38018",
      "decision_description": "Substantially Equivalent",
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}