FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Pulse Generator, Permanent, Implantable
PMA: P880086
·
Supplement: S167
·
Decision Jan 15, 2009
Classifications
1
FEI Numbers
35
Registration Numbers
35
Basic Information
- Device Name
- Pulse Generator, Permanent, Implantable
- Trade Name
- AFFINTY/IDENTITY/INTEGRITY/VICTORY FAMILY OF PACEMAKERS
- PMA Number
- P880086
- Supplement Number
- S167
- Device Class
- FDA Class 3
- Product Code
- NVZ
- Generic Name
- Pulse generator, permanent, implantable
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- January 15, 2009
- Date Received
- August 4, 2008
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MANUFACTURING PROCESS CHANGE FOR HYBRID ASSEMBLY.
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 |
|---|---|---|---|
| NVZ | Pulse Generator, Permanent, Implantable | FDA class 3 | Unknown |