Atlas FDA

PHYLAX IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM

FDA premarket approval P980023 · decided 1998-10-27

Approval details

PMA number
P980023
Trade name
PHYLAX IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM
Generic name
Implantable cardioverter defibrillator (non-CRT)
Applicant
Biotronik, Inc.
Date received
1998-06-08
Decision date
1998-10-27
Days to decision
141 days
Decision code
APPR
Product code
LWS
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
Approval for the Phylax Implantable Cardioverter Defibrillator (ICD) System: a) ICD PUlse Generator - Phylax XM ICD, model number 121491; Phylax XM Active Housing ICD, model number 121492; Phylax XM Replacement ICD, model number 121162 and mycroPhylax ICD, model number 121493; b) ICD Lead - SPS 75 Lead System, model number 120398; SL-ICD Lead Systems (SL-ICD 75/13, model number 120395, SL-ICD 75/16, model number 120396, SL-ICD 75/18, model number 120397, SL-ICD 100/13, model number 116414, SL-IC

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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