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

Stimulator, Hypoglossal Nerve, Implanted, Apnea

PMA: P130008 · Supplement: S004 · Decision Nov 6, 2014
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
S004
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
November 6, 2014
Date Received
October 7, 2014
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

INSTALL A NEW CURE AND PREHEAT OVEN AT THE CONTRACT MANUFACTURER¿S MEDTRONIC PUERTO RICO OPERATIONS COMPANY (MPROC) LOCATION.

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