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DROMOS DR/DR-A AND DROMOS SR/SR-B CARDIAC

FDA premarket approval P950037/S061 · decided 2008-06-09

Approval details

PMA number
P950037
Supplement
S061
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
DROMOS DR/DR-A AND DROMOS SR/SR-B CARDIAC
Generic name
Pulse generator, permanent, implantable
Applicant
Biotronik, Inc.
Date received
2008-05-21
Decision date
2008-06-09
Days to decision
19 days
Decision code
APPR
Product code
NVZ
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
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