Atlas FDA

Melody™ Transcatheter Pulmonary Valve

FDA premarket approval P140017/S032 · decided 2025-10-23

Approval details

PMA number
P140017
Supplement
S032
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Melody™ Transcatheter Pulmonary Valve
Generic name
Pulmonary valve prosthesis percutaneously delivered
Applicant
Medtronic, Inc.
Date received
2025-09-26
Decision date
2025-10-23
Days to decision
27 days
Decision code
OK30
Product code
NPV
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
modifications to the ethylene oxide sterilization cycle and additional sterilizers for the sub-tier supplier of sterile sutures used in valve assembly

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510(k) clearances by this applicant

RecordFirmDate
VitalFlow Set with Balance™ Biosurface (K261335)Medtronic, Inc.2026-07-31
Concerto Versa™ Detachable Coil (K261866)Medtronic, Inc.2026-06-24
Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae (K260195)Medtronic, Inc.2026-04-23
Retrograde Coronary Sinus Perfusion Cannulae (K253203)Medtronic, Inc.2026-02-19
Clearview Intracoronary Shunts (K253998)Medtronic, Inc.2026-01-20
Bio-Medicus Life Support Catheter and Introducer (K251831)Medtronic, Inc.2026-01-15
Concerto Versa™ Detachable Coil (K253511)Medtronic, Inc.2026-01-14
C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409)Medtronic, Inc.2025-12-19