Implantable Pacemaker Pulse-Generator
Basic Information
- Device Name
- Implantable Pacemaker Pulse-Generator
- Trade Name
- SELOX ST/JT STEROID-ELUTING PASSIVE-FIXATION ENDOCARDIAL PACKING LEAD MODELS SELOX ST 53, SELOX ST 60, SELOX JT 45 & 53
- PMA Number
- P950037
- Supplement Number
- S038
- Device Class
- FDA Class 3
- Product Code
- DXY
- Generic Name
- implantable pacemaker Pulse-generator
- Regulation Number
- 870.3610
- Medical Specialty
- Cardiovascular
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- November 10, 2004
- Date Received
- May 27, 2004
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR THE ADDITION OF A DRUG COLLAR TO THE PACING LEAD. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME SELOX ST/JT AND IS INDICATED AS FOLLOWS: SELOX ST AND SELOX JT STEROID ELUTING LEADS ARE DESIGNED FOR USE WITH IMPLANTABLE PULSE GENERATORS THAT REQUIRE PACING LEADS WITH A BIPOLAR 3.2 MM IS-1 CONNECTOR CONFIGURATION; THEY MAY BE USED WITH SINGLE OR DUAL CHAMBER PACING SYSTEMS. THE LEADS ARE DESIGNED FOR USE IN PATIENTS FOR WHOM SINGLE OR DUAL CHAMBER PULSE GENERATOR THERAPY IS MEDICALLY INDICATED. THIS INDICATION FOLLOWS THAT RECOMMENDED IN THE CLASS I DEFINITION OF THE ACC/AHA/NASPE TASK FORCE REPORT, ENTITLED "ACC/AHA/NASPE 2002 GUIDELINE UPDATE FOR IMPLANTATION OF CARDIAC PACEMAKERS AND ANTIARRHYTHMIA DEVICES: A REPORT OF THE AMERICAN COLLEGE OF CARDIOLOGY/AMERICAN HEART ASSOCIATION TASK FORCE ON PRACTICE GUIDELINES (ACC/AHA/NASPE COMMITTEE ON PACEMAKER IMPLANTATION)" (GREGORATOS ET AL. 2002).
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DXY | Implantable Pacemaker Pulse-Generator | FDA class 3 | Cardiovascular |