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.
Device | Exablate 4000 System |
Classification Name | Mr-guided Focused Ultrasound System |
Generic Name | Mr-guided Focused Ultrasound System |
Applicant | InSightec |
Date Received | 2018-04-23 |
Decision Date | 2018-05-09 |
PMA | P150038 |
Supplement | S007 |
Product Code | POH |
Docket Number | Premarket 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 Committee | Neurology |
Supplement Type | 30-day Notice |
Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | InSightec 5 Nahum Heth Street tirat-hacarmet 39120 |
Supplemental Filings
Supplement Number | Date | Supplement Type |
P150038 | | Original 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