Vitatron Impulse II Lead
FDA premarket approval P850089/S146 · decided 2020-03-06
Approval details
- PMA number
- P850089
- Supplement
- S146
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- 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
- 2020-02-20
- Decision date
- 2020-03-06
- Days to decision
- 15 days
- Decision code
- OK30
- Product code
- NVN
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Transfer two incoming inspection activities for device components from Medtronic Rice Creek to Medtronic Puerto Rico Operations Company Villalba/Juncos sites.
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