FDA PMA FDA Class 3 Approved 🇺🇸 United States

Device, Impotence, Mechanical/Hydraulic

PMA: P000006 · Supplement: S046 · Decision May 17, 2017
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
S046
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 17, 2017
Date Received
February 22, 2017
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for addition of a new insertion tool; update of pusher tool design; addition of shods supplied with kit; modification of package layout and material; use of new package denesting agent; and 2 year and 5 year shelf-life protocol.

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