FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Cochlear

PMA: P000025 · Supplement: S001 · Decision Jul 29, 2002
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Implant, Cochlear
Trade Name
COMBI 40+COCHLEAR IMPLANT SYSTEM,C40+S(COMPRESSED)ELECTRODE ARRAY/C40+ GB (SPLIT) ELECTRODE ARRAY
PMA Number
P000025
Supplement Number
S001
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 29, 2002
Date Received
December 18, 2001
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR THE MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM, C40+S (COMPRESSED) ELECTRODE ARRAY AND THE MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM, C40+ GB (SPLIT) ELECTRODE ARRAY.

Classifications

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

Product Code Device Name
MCM Implant, Cochlear