Exablate 4000 System

Mr-guided Focused Ultrasound System

FDA Premarket Approval P150038 S007

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Consolidate the two connector types of the 1. 5t head coil cables into a single connector type (p-type). The change is being made to maintain compatibility with the ge medical systems (ge) signa artist mr scanner.

DeviceExablate 4000 System
Classification NameMr-guided Focused Ultrasound System
Generic NameMr-guided Focused Ultrasound System
ApplicantInSightec
Date Received2018-04-23
Decision Date2018-05-09
PMAP150038
SupplementS007
Product CodePOH
Docket NumberPremarket Approval (PMA) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices Radia
Advisory CommitteeNeurology
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address InSightec 5 Nahum Heth Street tirat-hacarmet 39120

Supplemental Filings

Supplement NumberDateSupplement Type
P150038Original Filing
S024 2022-10-12 Normal 180 Day Track No User Fee
S023 2022-08-05 Real-time Process
S022
S021 2022-03-10 Real-time Process
S020 2022-03-08 30-day Notice
S019
S018
S017
S016
S015
S014 2021-03-31 Panel Track
S013 2020-10-23 Normal 180 Day Track
S012 2019-08-08 Normal 180 Day Track
S011 2019-03-26 30-day Notice
S010
S009
S008 2018-07-23 Normal 180 Day Track
S007 2018-04-23 30-day Notice
S006 2018-03-07 Panel Track
S005 2018-02-20 Normal 180 Day Track
S004 2017-08-16 Normal 180 Day Track No User Fee
S003 2017-03-28 Normal 180 Day Track
S002 2017-01-17 Normal 180 Day Track
S001 2016-08-03 Normal 180 Day Track No User Fee

NIH GUDID Devices

Device IDPMASupp
07290019402466 P150038 023
07290019402442 P150038 023

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.