Atlas FDA

Orsiro Mission Sirolimus Eluting Coronary Stent System

FDA premarket approval P170030/S048 · decided 2025-03-03

Approval details

PMA number
P170030
Supplement
S048
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Orsiro Mission Sirolimus Eluting Coronary Stent System
Generic name
Coronary drug-eluting stent
Applicant
Biotronik AG
Date received
2024-12-18
Decision date
2025-03-03
Days to decision
75 days
Decision code
APPR
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Bülach
Statement
Approval for dimensional modifications to the Luer lock connectors and manifolds as well as the corresponding injection molding equipment

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
PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER (K052757)Biotronik AG2005-10-28