Atlas FDA

DROMOS DR/SR RATE ADAPTIVE PACING SYSTEM

FDA premarket approval P950037/S139 · decided 2015-02-10

Approval details

PMA number
P950037
Supplement
S139
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
DROMOS DR/SR RATE ADAPTIVE PACING SYSTEM
Generic name
Pulse generator, permanent, implantable
Applicant
Biotronik, Inc.
Date received
2014-08-04
Decision date
2015-02-10
Days to decision
190 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR THE INVENTRA, IPERIA AND ITREVIA ICD AND CRT-D DEVICES AS WELL AS UPDATES TO NON-IMPLANTED COMPONENTS RENAMIC, PSW 1401.U AND THE HOME MONITORING SERVICE CENTER TO SUPPORT THE INTRODUCTION OF THE NEW ICD AND CRT-D DEVICES.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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