FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Intragastric For Morbid Obesity

PMA: P140008 · Supplement: S007 · Decision Aug 21, 2017
Classifications
1
FEI Numbers
12
Registration Numbers
12

Basic Information

Device Name
Implant, Intragastric For Morbid Obesity
Trade Name
Orbera Intragastric Balloon
PMA Number
P140008
Supplement Number
S007
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
August 21, 2017
Date Received
May 25, 2017
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol - OSB
Expedited Review
N

Advisory Committee Statement

Approval for revised protocol for the post-approval study (PAS) protocol.

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