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BELOS, CARDIAC AIRBAG, LEXOS, AND XELOS FAMILIES OF ICDS

FDA premarket approval P000009/S015 · decided 2005-06-22

Approval details

PMA number
P000009
Supplement
S015
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
BELOS, CARDIAC AIRBAG, LEXOS, AND XELOS FAMILIES OF ICDS
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Applicant
Biotronik, Inc.
Date received
2005-03-18
Decision date
2005-06-22
Days to decision
96 days
Decision code
APPR
Product code
MRM
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR THE IMPLANT CONTROL SYSTEM (ICS) 3000 PROGRAMMING SYSTEM, USING SOFTWARE VERSION 501.U FOR USE WITH THE BELOS, CARDIAC AIRBAG, LEXOS, AND XELOS FAMILIES OF ICDS.

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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