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CapSureFix Novus Lead, Vitatron Crystalline Active Fixation Lead

FDA premarket approval P930039/S264 · decided 2024-10-17

Approval details

PMA number
P930039
Supplement
S264
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CapSureFix Novus Lead, Vitatron Crystalline Active Fixation Lead
Generic name
Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
Applicant
Medtronic, Inc.
Date received
2024-10-04
Decision date
2024-10-17
Days to decision
13 days
Decision code
OK30
Product code
NVN
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
to update a silicone raw material incoming inspection procedure, location, and frequency

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