Atlas FDA

ACTIVA TREMOR CONTROL SYSTEM

FDA premarket approval P960009/S014 · decided 2000-11-28

Approval details

PMA number
P960009
Supplement
S014
Supplement type
Normal 180 Day Track
Supplement reason
Express GMP Supplement
Trade name
ACTIVA TREMOR CONTROL SYSTEM
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2000-10-26
Decision date
2000-11-28
Days to decision
33 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
APPROVAL FOR AN ALTERNATE MANUFACTURING FACILITY FOR THE MODEL 3387 AND MODEL 3389 DBS LEADS LOCATED AT MEDTRONIC NEUROLOGICAL PUERTO RICO, VILLALBA, PUERTO RICO.

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