Atlas FDA

ESTELLA AND EFFECTA PULSE GENERATORS

FDA premarket approval P950037/S092 · decided 2011-02-11

Approval details

PMA number
P950037
Supplement
S092
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ESTELLA AND EFFECTA PULSE GENERATORS
Generic name
Pulse generator, permanent, implantable
Applicant
Biotronik, Inc.
Date received
2010-12-13
Decision date
2011-02-11
Days to decision
60 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR THE ICS 3000 PROGRAMMER APPLICATION SOFTWARE VERSION PSW 1004.U, AND THE ESTELLA DR; ESTELLA DR-T; ESTELLA SR; ESTELLA SR-T; ECURO DR; ECURO DR-T; ECURO SR; ECURO SR-T; EFFECTA D; EFFECTA DR; EFFECTA S; AND EFFECTA SR. THE DEVICE, AS MODIFIED WILL BE MARKETED UNDER THE TRADE NAMES LISTED ABOVE, AND IS INDICATED FOR THE APPROVED INDICATION FOR USE.

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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