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

Stimulator, Hypoglossal Nerve, Implanted, Apnea

PMA: P130008 · Supplement: S045 · Decision Jul 25, 2019
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Stimulator, Hypoglossal Nerve, Implanted, Apnea
Trade Name
Inspire Upper Airway Stimulation System
PMA Number
P130008
Supplement Number
S045
Device Class
FDA Class 3
Product Code
MNQ
Generic Name
Stimulator, hypoglossal nerve, implanted, apnea
Medical Specialty
Unknown
Advisory Committee
Anesthesiology
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
July 25, 2019
Date Received
June 24, 2019
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Reduce the energy used in the seam welding process of the sensor component of the Model 4340 and Model 4323 Sensor Lead at the contract manufacturer Cirtec Medical.

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