FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Intragastric For Morbid Obesity

PMA: P140008 · Supplement: S017 · Decision Jun 3, 2019
Classifications
1
FEI Numbers
12
Registration Numbers
12

Basic Information

Device Name
Implant, Intragastric For Morbid Obesity
Trade Name
ORBERA Intragastric Balloon System
PMA Number
P140008
Supplement Number
S017
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
June 3, 2019
Date Received
March 4, 2019
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for revised labeling to include current post-market surveillance information, clarifications intended to enhance safety, and additional labeling pieces intended to enhance safety.

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