Atlas FDA

Activa Deep Brain Stimulation Therapy System

FDA premarket approval P960009/S382 · decided 2020-11-03

Approval details

PMA number
P960009
Supplement
S382
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Activa Deep Brain Stimulation Therapy System
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2020-08-21
Decision date
2020-11-03
Days to decision
74 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
Approval to add the use of tin-lead plating for the terminations of both ends of the TM8 capacitors and to change the solder paste stencil tooling for the 1411 capacitor size for the Model 97810 InterStim Micro INS to increase the amount of solder paste to match the mount used on other capacitor case sizes.

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