FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Ventricular (Assist) Bypass

PMA: P160054 · Supplement: S068 · Decision Dec 14, 2023
Classifications
1
FEI Numbers
21
Registration Numbers
21

Basic Information

Device Name
Ventricular (Assist) Bypass
Trade Name
HeartMate 3™ Left Ventricular Assist System
PMA Number
P160054
Supplement Number
S068
Device Class
FDA Class 3
Product Code
DSQ
Generic Name
Ventricular (assist) bypass
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
December 14, 2023
Date Received
November 17, 2023
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Change for the inspection of the HeartMate 14 Volt Li-Ion Battery from 100% Sampling to AQL Sampling at Abbott Receiving Inspection.

Classifications

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

Product Code Device Name
DSQ Ventricular (Assist) Bypass