A Clinical Trial to Evaluate the Safety and Efficacy of Neuromodulation Using 'ExAblate 4000 Type 2.1' in Patients With Psychostimulant Use Disorder(PUD)

Inclusion Criteria: 1. Adults between the ages of 19 and 60 2. Subject is diagnosed with a DSM-5 psychostimulant\* use disorder (PUD) by a board certified psychiatrist. \*Psychostimulants: Methamphetamine, cocaine, and other stimulants 3. Subject is currently receiving standard substance use disorder inpatient treatment or an intensive outpatient program 4. Subject has been off psychostimulants and other illicit drugs, confirmed via urine toxicology screen 5. Subject has not regularly used illegal drugs other than psychostimulants more than once a month in the past six months 6. The NAc is apparent on MRI such that treatment targeting can be performed directly (visible on MRI) and indirectly (using other anatomical structures for measurements) 7. Subject is able to communicate sensations during the investigational procedure 8. Subject has made a voluntary decision to participate in this clinical trial and has given written consent. 9. Subject is willing to comply to the protocol Exclusion Criteria: 1. Subject with standard contraindication for MR imaging, such as non-MRI compatible implanted metallic devices. 2. Subject with known allergies to the MRI contrast agent gadolinium (Gadovist®) or contraindication (such as untreated hypokalemia). 3. Subject who are unable or unwilling to tolerate the required prolonged stationary position during treatment (approximately 2-3 hours) 4. More than 30% of the skull area traversed by the sonication pathyway is covered by scars, scalp disorder (e.g., eczema), or atrophy of the scalp. 5. Subject with implanted objects in the skull or brain 6. Subject diagnosed with advanced kidney disease or on dialysis 7. Subjet with impaired renal function with estimated glomerular filtration rate less than 30 mL/min/1.73 m 2 8. Subject with known unstable cardiac status or severe hypertension including: * Documented myocardial infarction within six months of enrollment * Unstable angina on medication * Unstable or worsening congestive heart failure * Left ventricular ejection fraction (LVEF) below the lower limit of normal * History of hemodynamically unstable cardiac arrhythmias * Cardiac pacemaker * Severe hypertension (diastolic blood pressure over 100 on medication) 9. Subject has a history of abnormal bleeding or coagulopathy 10. Subject is receiving anticoagulant (e.g., warfarin) or antiplatelet (e.g., aspirin) therapy within one week of focused ultrasound procedure or drugs known to increase risk of hemorrhage (e.g., Avastin) within one month of focused ultrasound procedure 11. Subject has blood coagulation test results outside the normal range * PLT\<100,000/μL * PT\>13.9 seconds or PTT\>37.5 seconds * INR\>1.2 12. Subject with cerebrovascular disease as determined by MRI according to Fazekas score 13. Subject with a past or current diagnosis of schizophrenia, psychotic disorder, bipolar disorder, or untreated depression other than one determined to be substance induced 14. Score of greater than 17 on the Hamilton Depression Rating Scale (HAM-D) or increased risk of suicide based on any positive response regarding passive or active suicidal ideation with or without intent over the past 3 months or lifetime history of active suicidal ideation with intent on the Columbia-Suicide Severity Rating Scale (C-SSRS) at baseline 15. Diagnosis of dementia or any other disorder which has led to a clinically significant cognitive impairment (assessed via NIHTB-CB) 16. Subject with brain tumors 17. Subject with chronic pulmonary disorders e.g. severe emphysema, pulmonary vasculitis, or other casues of reduced pulmonary vascular cross-sectional area. 18. Any known CNS infection or infection with the human immunodeficiency virus (HIV) 19. Subject who has had deep brain stimulation or a prior stereostatic ablation of the NAc, basal ganglia, or thalamus 20. Subject who has been administered botulinum toxins into to the arm, neck, or face for 5 months prior to baseline 21. Subject unwilling to refrain from using illicit drugs while participating in this clinical trial 22. Subject is pregnant or nursing women 23. For women of childbearing potential\*, who do not agree to use clinically appropriate contraception\*\* for the duration of the clinical trial \*Definition of women of childbearing age: means women who have experienced menarche, have not been surgically sterilized (hysterectomy or bilateral oophorectomy), or are not post-menopausal, defined as amenorrhea for 12 months or more for no other reason. \*\*Clinically appropriate contraception: defined as "\[intrauterine device (e.g., Loop, Mirena), chemical barrier method (spermicide), or subdermal implantable contraceptive device (e.g., Implanon)\] + physical barrier method (male or female)" for women, tubal surgery, or laparoscopic contraception (a type of tubal ligation). 24. Other, if the investigator determines that participation in the clinical trial is inappropriate ethically or because it may affect the outcome of the clinical trial