NeuroTrigger Basic (NTB)
K-Number: K223027 · 2023-10-10
ApplicantNeurotrigger
Decision Date2023-10-10
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
NeuroTrigger Basic (NTB) is a medical device manufactured by Neurotrigger. It received FDA 510(k) clearance on 2023-10-10 under approval number K223027. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NeuroTrigger Basic (NTB)?
NeuroTrigger Basic (NTB) is a medical device that received FDA 510(k) clearance on 2023-10-10. It is manufactured by Neurotrigger. The 510(k) number is K223027.
When was NeuroTrigger Basic (NTB) approved by the FDA?
NeuroTrigger Basic (NTB) received FDA 510(k) clearance on 2023-10-10, under approval number K223027.
What company makes NeuroTrigger Basic (NTB)?
NeuroTrigger Basic (NTB) is manufactured by Neurotrigger.
What is the FDA product code for NeuroTrigger Basic (NTB)?
The FDA product code for NeuroTrigger Basic (NTB) is IPF.
Related Devices (Code: IPF)
K160614Xcite Clinical StationRestorative Therapies, Inc.
K163067CyMedica e-vive System; CY-1000Cymedica Orthopedics, Inc.
K160992HPM-6000BTL Industries, Inc.
K151922StimSox(TM) SystemStimmed, LLC
K153696Chattanooga Revolution WirelessDjo, LLC
K160299geko(TM) Plus R-2 Neuromuscular StimulatorFirstkind Limited
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.