Atlas FDA

ACTIVITRAX MODELS 8400, 8402, 8403

FDA premarket approval P850051/S016 · decided 1988-08-11

Approval details

PMA number
P850051
Supplement
S016
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ACTIVITRAX MODELS 8400, 8402, 8403
Generic name
Pulse-generator, single chamber, sensor driven, implantable
Applicant
Medtronic, Inc.
Date received
1988-08-03
Decision date
1988-08-11
Days to decision
8 days
Decision code
APPR
Product code
LWO
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN

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510(k) clearances by this applicant

RecordFirmDate
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Retrograde Coronary Sinus Perfusion Cannulae (K253203)Medtronic, Inc.2026-02-19
Clearview Intracoronary Shunts (K253998)Medtronic, Inc.2026-01-20
Bio-Medicus Life Support Catheter and Introducer (K251831)Medtronic, Inc.2026-01-15
Concerto Versa™ Detachable Coil (K253511)Medtronic, Inc.2026-01-14
C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409)Medtronic, Inc.2025-12-19