Nexstim Navigated Brain Therapy (NBT) System 2
K-Number: K171902 · 2017-11-10
Device Summary
Frequently Asked Questions
What is the Nexstim Navigated Brain Therapy (NBT) System 2?
Nexstim Navigated Brain Therapy (NBT) System 2 is a medical device that received FDA 510(k) clearance on 2017-11-10. The listed applicant is Nexstim Plc. The 510(k) number is K171902.
When did Nexstim Navigated Brain Therapy (NBT) System 2 receive FDA 510(k) clearance?
Nexstim Navigated Brain Therapy (NBT) System 2 received FDA 510(k) clearance on 2017-11-10, under 510(k) number K171902.
Who is the listed applicant for Nexstim Navigated Brain Therapy (NBT) System 2?
The FDA 510(k) record lists Nexstim Plc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nexstim Navigated Brain Therapy (NBT) System 2?
The FDA product code for Nexstim Navigated Brain Therapy (NBT) System 2 is OBP.
Other records listing Nexstim Plc as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OBP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.