FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Implant, Intragastric For Morbid Obesity
PMA: P140008
·
Supplement: S003
·
Decision May 23, 2016
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
- 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
- May 23, 2016
- Date Received
- September 18, 2015
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
approval for a manufacturing site located at Apollo Endosurgery, Building 13.3, Zona Franca Coyol, Alajuela, Costa Rica
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LTI | Implant, Intragastric For Morbid Obesity | FDA class 3 | Unknown |