FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Mr-Guided Focused Ultrasound System
PMA: P150038
·
Supplement: S001
·
Decision Sep 29, 2016
Classifications
1
FEI Numbers
4
Registration Numbers
4
Basic Information
- Device Name
- Mr-Guided Focused Ultrasound System
- Trade Name
- EXABLATE NEURO THALAMOTOMY
- PMA Number
- P150038
- Supplement Number
- S001
- Device Class
- FDA Class 3
- Product Code
- POH
- Generic Name
- MR-guided focused ultrasound system
- Medical Specialty
- Unknown
- Advisory Committee
- Neurology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 29, 2016
- Date Received
- August 3, 2016
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the protocol for the ODE Lead PMA Post-Approval Study 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 |
|---|---|---|---|
| POH | Mr-Guided Focused Ultrasound System | FDA class 3 | Unknown |