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Ilivia 7 HF-T, Intica 7/5 HF-T, Acticor 7 HF-T, Rivacor 7/5/3 HF-T, Ilivia 7 HF-T QP, Initca 7 HF-T QP, Acticor 7 HF-T Q

FDA premarket approval P050023/S190 · decided 2025-03-10

Approval details

PMA number
P050023
Supplement
S190
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Ilivia 7 HF-T, Intica 7/5 HF-T, Acticor 7 HF-T, Rivacor 7/5/3 HF-T, Ilivia 7 HF-T QP, Initca 7 HF-T QP, Acticor 7 HF-T Q
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Applicant
Biotronik, Inc.
Date received
2024-12-10
Decision date
2025-03-10
Days to decision
90 days
Decision code
APPR
Product code
MRM
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
approval to expand MR conditional scan durations for system configurations including Pamira and Plexa ICD leads

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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