FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Intragastric For Morbid Obesity

PMA: P070009 · Supplement: S013 · Decision Mar 31, 2011
Classifications
1
FEI Numbers
12
Registration Numbers
12

Basic Information

Device Name
Implant, Intragastric For Morbid Obesity
Trade Name
REALIZE ADJUSTABLE GASTRIC BANDS WITH INJECTION PORT & APPLIER
PMA Number
P070009
Supplement Number
S013
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
March 31, 2011
Date Received
February 8, 2011
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A DEVICE CHANGE TO MODIFY THE SILICONE MATERIAL USED FOR THE INJECTION PORT SEPTUM AND INJECTION PORT CONNECTOR SLEEVE COMPONENTS, ALONG WITH A MINOR ASSOCIATED LABELING MODIFICATION.

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