PMA P140012S012
- Device
- ReShape Integrated Dual Balloon System
- Applicant
- Boston Scientific Corporation
- PMA number
- P140012
- Supplement
- S012
- Product code
- LTI
- Decision date
- 2018-05-30
- Classification
- Implant, Intragastric For Morbid Obesity
- Generic name
- IMPLANT, INTRAGASTRIC FOR MORBID OBESITY
- Approval order statement
- Approval of the revised protocol of the post-approval study protocol.
Current openFDA PMA Record#
- Device
- ReShape Integrated Dual Balloon System
- Applicant
- Boston Scientific Corporation
- PMA number
- P140012
- Supplement
- S012
- Product code
- LTI
- Generic name
- IMPLANT, INTRAGASTRIC FOR MORBID OBESITY
- Decision date
- 2018-05-30
- Decision code
- APPR
- Date received
- 2018-02-26
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Postapproval Study Protocol - OSB
- Approval order statement
- Approval of the revised protocol of the post-approval study protocol.