FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Auditory Brainstem

PMA: P000015 · Supplement: S041 · Decision Jul 2, 2020
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Implant, Auditory Brainstem
Trade Name
Nucleus Auditory Brainstem Implant
PMA Number
P000015
Supplement Number
S041
Device Class
FDA Class 3
Product Code
MHE
Generic Name
Implant, auditory brainstem
Medical Specialty
Unknown
Advisory Committee
Ear, Nose, Throat
Decision
Approved
Decision Code
APPR
Decision Date
July 2, 2020
Date Received
November 13, 2019
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the Kanso 2 Sound Processor and associated accessories, Nucleus 7 for Nucleus 22, SmartNav System including SmartNav App and CP1150S Surgical Processor, and Custom Sound Pro.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MHE Implant, Auditory Brainstem