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
POH Mr-Guided Focused Ultrasound System