FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Hypoglossal Nerve, Implanted, Apnea

PMA: P130008 · Supplement: S021 · Decision Jun 23, 2017
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Stimulator, Hypoglossal Nerve, Implanted, Apnea
Trade Name
Inspire II Upper Airway Stimulator
PMA Number
P130008
Supplement Number
S021
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
June 23, 2017
Date Received
March 29, 2017
Supplement Type
Normal 180 Day Track
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval to expand the Apnea Hypopnea Index (AHI) range from 20 to 65, to 15 to 65 events per hour.

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