CapSure SP Novus Lead, Vitatron Impulse II Lead
FDA premarket approval P850089/S164 · decided 2023-03-28
Approval details
- PMA number
- P850089
- Supplement
- S164
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- CapSure SP Novus Lead, Vitatron Impulse II Lead
- Generic name
- Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2023-03-20
- Decision date
- 2023-03-28
- Days to decision
- 8 days
- Decision code
- OK30
- Product code
- NVN
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Change the Crimp Core component inspection from a manual to an automatic process at Lake Region Medical.
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