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IFORIA 5/7, ILESTO 57/, INVENTRA 7, IPERIA 5/7, ITREVIA 5/7, ILIVIA 5/7, INTICA 5/7, INLEXA 5/7, LUMAX 300/340 and 500/5

FDA premarket approval P050023/S124 · decided 2018-10-22

Approval details

PMA number
P050023
Supplement
S124
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
IFORIA 5/7, ILESTO 57/, INVENTRA 7, IPERIA 5/7, ITREVIA 5/7, ILIVIA 5/7, INTICA 5/7, INLEXA 5/7, LUMAX 300/340 and 500/5
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Applicant
Biotronik, Inc.
Date received
2018-08-22
Decision date
2018-10-22
Days to decision
61 days
Decision code
APPR
Product code
MRM
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
Approval for an updated version of Renamic and ICS 3000 programmer software, PSW 1802.U.

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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