{
  "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": "2026-10-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 15
    }
  },
  "results": [
    {
      "pma_number": "P140019",
      "supplement_number": "S004",
      "applicant": "Cerapedics, LLC",
      "street_1": "11025 Dover St., Suite 1600",
      "street_2": "",
      "city": "Westminster",
      "state": "CO",
      "zip": "80021",
      "zip_ext": "",
      "generic_name": "Filler, bone void, synthetic peptide",
      "trade_name": "i-FACTOR Peptide Enhanced Bone Graft",
      "product_code": "NOX",
      "advisory_committee": "OR",
      "advisory_committee_description": "Orthopedic",
      "supplement_type": "Normal 180 Day Track No User Fee",
      "supplement_reason": "Labeling Change - PAS",
      "expedited_review_flag": "N",
      "date_received": "2020-06-15",
      "decision_date": "2020-07-22",
      "docket_number": "",
      "decision_code": "APPR",
      "ao_statement": "Approval for updated labeling to include the results from the completed 72-month follow-up post-approval study.",
      "openfda": {
        "device_name": "Filler, Bone Void, Synthetic Peptide",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
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