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

Stimulator, Hypoglossal Nerve, Implanted, Apnea

PMA: P130008 · Supplement: S105 · Decision Dec 8, 2023
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Stimulator, Hypoglossal Nerve, Implanted, Apnea
Trade Name
4340 Sensing Lead and 4063 Stimulation Lead
PMA Number
P130008
Supplement Number
S105
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
December 8, 2023
Date Received
November 9, 2023
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

approval for updates to work instructions used to manufacture the Model 4340 Sensing Lead and 4063 Stimulation 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