FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Intragastric For Morbid Obesity

PMA: P160001 · Supplement: S003 · Decision Apr 25, 2017
Classifications
1
FEI Numbers
12
Registration Numbers
12

Basic Information

Device Name
Implant, Intragastric For Morbid Obesity
Trade Name
OBALON BALLOON SYSTEM
PMA Number
P160001
Supplement Number
S003
Device Class
FDA Class 3
Product Code
LTI
Generic Name
IMPLANT, INTRAGASTRIC FOR MORBID OBESITY
Medical Specialty
Unknown
Advisory Committee
Gastroenterology, Urology
Decision
Approved
Decision Code
APPR
Decision Date
April 25, 2017
Date Received
November 16, 2016
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the additional of a plant-based capsule material option.

Classifications

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

Product Code Device Name
LTI Implant, Intragastric For Morbid Obesity