Atlas FDA

BELOS VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM

FDA premarket approval P980023/S004 · decided 2001-07-12

Approval details

PMA number
P980023
Supplement
S004
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
BELOS VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM
Generic name
TESTER, PACEMAKER ELECTRODE FUNCTION
Applicant
Biotronik, Inc.
Date received
2001-04-27
Decision date
2001-07-12
Days to decision
76 days
Decision code
APPR
Product code
DTA
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR A NEW ICD SYSTEM THAT INCLUDES THE FOLLOWING: BELOS VR ICD (MODEL 330 444), BELOS TEST HOUSING (MODEL 331 116), AND BELOS VR PHYLAX XM/MYCROPHYLAX/PHYLAX 06/TMS 1000 APPLICATION SOFTWARE 1-K01.0.A (MODEL 338 045). THE DEVICE, AS MODIFIED IS INDICATED TO PROVIDE VENTRICULAR ANTITACHYCARDIA PACING AND VENTRICULAR DEFIBRILLATION, FOR AUTOMATED TREATMENT OF LIFE-THREATENING VENTRICULAR ARRHYTHMIAS.

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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