Atlas FDA

Inspire Implantable Pulse Generator

FDA premarket approval P130008/S058 · decided 2020-09-16

Approval details

PMA number
P130008
Supplement
S058
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Inspire Implantable Pulse Generator
Generic name
Stimulator, hypoglossal nerve, implanted, apnea
Applicant
Inspire Medical Systems
Date received
2020-08-20
Decision date
2020-09-16
Days to decision
27 days
Decision code
OK30
Product code
MNQ
Advisory committee
Anesthesiology
Expedited review
No
Location
Maple Grove, MN
Statement
Change to the cleaning process of Model 3028 IPG involving the replacement of trichloroethylene with an alcohol-based solvent.

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