Atlas FDA

PHILOS AND AXIOS FAMILY OF PULSE GENERATORS

FDA premarket approval P950037/S051 · decided 2007-08-31

Approval details

PMA number
P950037
Supplement
S051
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
PHILOS AND AXIOS FAMILY OF PULSE GENERATORS
Generic name
Pulse generator, permanent, implantable
Applicant
Biotronik, Inc.
Date received
2007-04-10
Decision date
2007-08-31
Days to decision
143 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR CHANGES TO THE INTEGRATED CIRCUIT PACKAGING, CIRCUIT BOARD SUBSTRATE, HEADER ASSEMBLY, AND THE TEL 3000 INTERFACE IN THE PHILOS AND AXIOS FAMILY OF PULSE GENERATORS.

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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