FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Cochlear

PMA: P000025 · Supplement: S106 · Decision Jul 2, 2019
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Implant, Cochlear
Trade Name
+FLEX Active Electrode and Insertion Electrode (IE) FLEX
PMA Number
P000025
Supplement Number
S106
Device Class
FDA Class 3
Product Code
MCM
Generic Name
Implant, cochlear
Medical Specialty
Unknown
Advisory Committee
Ear, Nose, Throat
Decision
Approved
Decision Code
APPR
Decision Date
July 2, 2019
Date Received
December 17, 2018
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval order should be issued for the +FLEX26 Active Electrode and Insertion Electrode (IE) FLEX26.

Classifications

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

Product Code Device Name
MCM Implant, Cochlear