Atlas FDA

Activa® Deep Brain Stimulation Therapy System

FDA premarket approval P960009/S446 · decided 2023-02-02

Approval details

PMA number
P960009
Supplement
S446
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Activa® Deep Brain Stimulation Therapy System
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2023-01-20
Decision date
2023-02-02
Days to decision
13 days
Decision code
OK30
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
Implement manufacturing process changes at an external supplier in order to manufacturing different sized TBC series tantalum capacitors.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
VitalFlow Set with Balance™ Biosurface (K261335)Medtronic, Inc.2026-07-31
Concerto Versa™ Detachable Coil (K261866)Medtronic, Inc.2026-06-24
Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae (K260195)Medtronic, Inc.2026-04-23
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