{
  "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": "2026-10-05",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "pma_number": "P060039",
      "supplement_number": "",
      "applicant": "Medtronic, Inc.",
      "street_1": "8200 Coral Sea St. N.E",
      "street_2": "Ms Mvs11",
      "city": "Mounds View",
      "state": "MN",
      "zip": "55112",
      "zip_ext": "",
      "generic_name": "Drug eluting permanent left ventricular (lv) pacemaker electrode",
      "trade_name": "ATTAIN STARFIX MODEL 4195 LEAD",
      "product_code": "OJX",
      "advisory_committee": "CV",
      "advisory_committee_description": "Cardiovascular",
      "supplement_type": "",
      "supplement_reason": "",
      "expedited_review_flag": "N",
      "date_received": "2006-12-27",
      "decision_date": "2008-06-13",
      "docket_number": "08M-0478",
      "fed_reg_notice_date": "2008-08-27",
      "decision_code": "APPR",
      "ao_statement": "APPROVAL FOR THE ATTAIN STARFIX MODEL 4195 LEAD.  THE ATTAIN STARFIX MODEL 4195 STEROID ELUTING, TRANSVENOUS LEAD WITH DEPLOYABLE LOBE FIXATION IS INTENDED FOR CHRONIC PACING AND SENSING OF THE LEFT VENTRICLE VIA THE CARDIAC VEIN, WHEN USED IN CONJUNCTION WITH A COMPATIBLE IMPLANTABLE PULSE GENERATOR OR IMPLANTABLE CARDIAC DEFIBRILLATOR.",
      "openfda": {
        "registration_number": [
          "9610139",
          "2182208",
          "2124215",
          "3006705815",
          "2017865",
          "3009380063",
          "2649622",
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          "3000206435",
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          "3018094310",
          "3002807576"
        ],
        "device_name": "Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}