FDA PMA FDA Class 3 Approved 🇺🇸 United States

Drug-Eluting Peripheral Transluminal Angioplasty Catheter

PMA: P130024 · Supplement: S034 · Decision May 14, 2020
Classifications
1
FEI Numbers
26
Registration Numbers
26

Basic Information

Device Name
Drug-Eluting Peripheral Transluminal Angioplasty Catheter
Trade Name
Lutonix 035 Drug Coated Balloon PTA Catheter
PMA Number
P130024
Supplement Number
S034
Device Class
FDA Class 3
Product Code
ONU
Generic Name
Drug-Eluting Peripheral Transluminal Angioplasty Catheter
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
May 14, 2020
Date Received
March 12, 2020
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for a new tie-layer material in the inner catheter shaft.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ONU Drug-Eluting Peripheral Transluminal Angioplasty Catheter