LEAD ASSEMBLY
FDA premarket approval P030036/S007 · decided 2008-07-17
Approval details
- PMA number
- P030036
- Supplement
- S007
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- LEAD ASSEMBLY
- Generic name
- Permanent defibrillator electrodes
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2008-06-17
- Decision date
- 2008-07-17
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- NVY
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- MOVING MANUFACTURING LOCATIONS WITHIN THE SAME FACILITY.
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