Atlas FDA

PHYLAX IMPLANTABLE CARDIOVERTER DIFIBRILLATOR

FDA premarket approval P980023/S033 · decided 2008-06-09

Approval details

PMA number
P980023
Supplement
S033
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
PHYLAX IMPLANTABLE CARDIOVERTER DIFIBRILLATOR
Generic name
Implantable cardioverter defibrillator (non-CRT)
Applicant
Biotronik, Inc.
Date received
2008-05-21
Decision date
2008-06-09
Days to decision
19 days
Decision code
APPR
Product code
LWS
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR MINOR MECHANICAL CHANGES TO THE ICS 3000 PROGRAMMER INCLUDING REMOVAL OF MAGNETS FROM THE PGH WAND AND REPLACEMENT OF AN EXISTING CONNECTOR AS WELL AS ASSOCIATED LABELING UPDATES.

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510(k) clearances by this applicant

RecordFirmDate
BIOMONITOR IV (471155) (K261074)Biotronik, Inc.2026-05-01
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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