FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Implant, Intragastric For Morbid Obesity
PMA: P140008
·
Supplement: S014
·
Decision Nov 28, 2018
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
- S014
- 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
- November 28, 2018
- Date Received
- October 2, 2018
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the 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 | Device Class | Medical Specialty |
|---|---|---|---|
| LTI | Implant, Intragastric For Morbid Obesity | FDA class 3 | Unknown |