FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
PMA: P080006
·
Supplement: S002
·
Decision Apr 1, 2011
Classifications
1
FEI Numbers
22
Registration Numbers
22
Basic Information
- Device Name
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
- Trade Name
- MEDTRONIC ATTAIN ABILITY PLUS MODEL 4296 LEAD
- PMA Number
- P080006
- Supplement Number
- S002
- Device Class
- FDA Class 3
- Product Code
- OJX
- Generic Name
- Drug eluting permanent left ventricular (lv) pacemaker electrode
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- April 1, 2011
- Date Received
- June 10, 2009
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR THE ATTAIN ABILITY¿ PLUS MODEL 4296 LEAD.
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 |
|---|---|---|---|
| OJX | Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode | FDA class 3 | Unknown |