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MEDTRONIC TRANSVENE LEAD SYSTEM

FDA premarket approval P920015/S008 · decided 1995-12-07

Approval details

PMA number
P920015
Supplement
S008
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MEDTRONIC TRANSVENE LEAD SYSTEM
Generic name
Implantable cardioverter defibrillator (non-CRT)
Applicant
Medtronic, Inc.
Date received
1995-08-10
Decision date
1995-12-07
Days to decision
119 days
Decision code
APPR
Product code
LWS
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR USE OF AN ALTERNATE STERILIZATION PROCESS AND A MODIFICATION TO THE DISTAL END OF THE TRANSVENE LEADS

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510(k) clearances by this applicant

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C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409)Medtronic, Inc.2025-12-19