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

Stimulator, Hypoglossal Nerve, Implanted, Apnea

PMA: P130008 · Supplement: S059 · Decision Sep 24, 2020
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Stimulator, Hypoglossal Nerve, Implanted, Apnea
Trade Name
Inspire Upper Airway Stimulation
PMA Number
P130008
Supplement Number
S059
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
September 24, 2020
Date Received
August 26, 2020
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Implementation of a new capillary tool for wire bonding process for the membrane subassembly used in Model 4340 sensing lead.

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