FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Hypoglossal Nerve, Implanted, Apnea

PMA: P130008 · Supplement: S033 · Decision May 15, 2018
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Stimulator, Hypoglossal Nerve, Implanted, Apnea
Trade Name
Inspire Upper Airway Stimulator
PMA Number
P130008
Supplement Number
S033
Device Class
FDA Class 3
Product Code
MNQ
Generic Name
Stimulator, hypoglossal nerve, implanted, apnea
Medical Specialty
Unknown
Advisory Committee
Anesthesiology
Decision
Approved
Decision Code
APPR
Decision Date
May 15, 2018
Date Received
February 14, 2018
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for proposed changes to the Inspire systems MRI Guidelines Manual.

Classifications

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

Product Code Device Name
MNQ Stimulator, Hypoglossal Nerve, Implanted, Apnea