Neuronetics, Inc. announced that it plans to release second quarter 2018 financial results prior to market open on Tuesday, August 14, 2018. Chris Thatcher, Chief Executive Officer, and Peter Donato, Chief Financial Officer, will host a conference call to review the Company’s results at 8:30 a.m. Eastern Time the same day.
MALVERN, Pa., July 31, 2018 (GLOBE NEWSWIRE) -- Neuronetics, Inc. (NASDAQ:STIM), a commercial-stage medical device company focused on designing, developing, and manufacturing products that improve the quality of life for patients who suffer from psychiatric disorders and the maker of the NeuroStar® Advanced Therapy System, a non-drug, office-based therapy cleared by the FDA in 2008 to treat adult patients with Major Depressive Disorder who have not seen success with at least one antidepressant medication in the current episode, today announced that it plans to release second quarter 2018 financial results prior to market open on Tuesday, August 14, 2018. Chris Thatcher, Chief Executive Officer, and Peter Donato, Chief Financial Officer, will host a conference call to review the Company’s results at 8:30 a.m. Eastern Time the same day. The call will be concurrently webcast.
To listen to the conference call on your telephone, please dial (877) 472-8990 for United States callers or +1 (629) 228-0778 for international callers and reference confirmation code 4873699, approximately ten minutes prior to start time. To access the live audio webcast or subsequent archived recording, visit the Investor Relations section of Neuronetics’ website at www.neuronetics.com. The replay will be available on the Company’s website for approximately 60 days.
About Neuronetics, Inc.
Neuronetics is a commercial stage medical technology company focused on designing, developing and marketing products that improve the quality of life for patients who suffer from psychiatric disorders. Our first commercial product, the NeuroStar Advanced Therapy System, is a non-invasive and non-systemic office-based treatment that uses transcranial magnetic stimulation, or TMS, to create a pulsed, MRI-strength magnetic field that induces electrical currents designed to stimulate specific areas of the brain associated with mood. The system is cleared by the United States Food and Drug Administration, or FDA. NeuroStar TMS Therapy is indicated for the treatment of major depressive disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. Additional information can be found at www.neuronetics.com.
Contacts:
For Investor Inquiries:
Mark R. Klausner
Westwicke Partners
443-213-0501
ir@neuronetics.com
For Media Inquiries:
Leanne Scott Brown
Vault Communications
610-455-2742
Lbrown@vaultcommunications.com
