Atlas FDA

ICS 3000 IMPLANT CONTROL SYSTEM

FDA premarket approval P950037/S055 · decided 2007-12-07

Approval details

PMA number
P950037
Supplement
S055
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ICS 3000 IMPLANT CONTROL SYSTEM
Generic name
Pulse generator, permanent, implantable
Applicant
Biotronik, Inc.
Date received
2007-10-23
Decision date
2007-12-07
Days to decision
45 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR CHANGES TO THE ICS 300 PROGRAMMER HEAD, TECHNICAL MANUAL, AND THE PGH BLUE FOIL LABEL.

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510(k) clearances by this applicant

RecordFirmDate
BIOMONITOR IV (471155) (K261074)Biotronik, Inc.2026-05-01
Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo-18 Peripheral Dilatation Catheters; Passeo-14 Peripheral Dilatation Catheter; Oscar Peripheral Multifunctional Catheter System; Pantera Pro Percutaneous Transluminal Coronary Angioplasty Catheter; Pantera LEO Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter (K250706)Biotronik, Inc.2025-04-04
Pantera Pro; Pantera LEO (K242969)Biotronik, Inc.2024-10-25
Selectra 3D Lead Delivery System (443624-443629, 451789-451791); Selectra Slitter Tool (383119); Selectra Accessory Kit (375518) (K240787)Biotronik, Inc.2024-09-12
Oscar Peripheral Multifunctional Catheter system (K241711)Biotronik, Inc.2024-07-11
BIOMONITOR IV (K230375)Biotronik, Inc.2023-05-19
Passeo-35 Xeo Peripheral Dilatation Catheter (K222065)Biotronik, Inc.2023-02-16
BIOMONITOR IIIm, BIOMONITOR III (K221856)Biotronik, Inc.2022-07-27