FDA PMA FDA Class 3 Approved 🇺🇸 United States

Device, Impotence, Mechanical/Hydraulic

PMA: P000006 · Supplement: S070 · Decision May 28, 2025
Classifications
1
FEI Numbers
5
Registration Numbers
5

Basic Information

Device Name
Device, Impotence, Mechanical/Hydraulic
Trade Name
Titan Inflatable Penile Prosthesis
PMA Number
P000006
Supplement Number
S070
Device Class
FDA Class 3
Product Code
FHW
Generic Name
Device, impotence, mechanical/hydraulic
Regulation Number
876.3350
Medical Specialty
Gastroenterology, Urology
Advisory Committee
Gastroenterology, Urology
Decision
Approved
Decision Code
APPR
Decision Date
May 28, 2025
Date Received
November 21, 2024
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

approval for an alternate sterilization site for the Titan Inflatable Penile Prosthesis Assembly Kits and Rear Tips Extenders at Sterigenics, West Memphis, Arkansas.

Classifications

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

Product Code Device Name
FHW Device, Impotence, Mechanical/Hydraulic