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- LEMHuman Lyophilized Dura Mater2Product Code
- LGWStimulator, Spinal-Cord, Totally Implanted For Pain Relief3Product Code
- LHYElectrode, Stabilized Epidural Spinal3Product Code
- LIIMonitor, Intracranial Pressure, Implanted3Product Code
- LKWLaser, Neurosurgical3Product Code
- LLEStimulator, Spinal-Cord, Implanted For Peripheral Vascular Disease3Product Code
- LLFLaser, Neurosurgical, Argon3Product Code
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- LMEMonitor, Blood-Flow, Cerebral, Thermal Diffusion3Product Code
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- LYIStimulator, Subcortical, Implanted For Epilepsy3Product Code
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- KGFAdhesive, Tissue For Aneurysmorrhaphy3Product Code
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- MFRStimulator, Brain, Implanted, For Behavior ModificationFProduct Code
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- MKDStimulator, Functional Walking Neuromuscular, Non-Invasive3Product Code
- MLQInhibitor, Peridural Fibrosis (Adhesion Barrier)3Product Code
- MRUImplanted Subcortical Electrical Stimulator (Motor Disorders)FProduct Code
- MUZStimulator, Autonomic Nerve, Implanted (Depression)3Product Code
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- NJEIntracranial Neurovascular StentFProduct Code
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- OBAPolymerizing, Neurovascular Embolization MaterialFProduct Code
- OLMDeep Brain Stimulator For Obsessive Compulsive Disorder (Ocd)FProduct Code
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- SBGIn Situ Polymerizing Peripheral Nerve Cap2Product Code
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NTX100 Tonic Motor Activation (NTX100 ToMAc) System
- Page Type
- Cleared 510(K)
- PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- DEN220059
- 510(k) Type
- Direct
- Applicant
- Noctrix Health, Inc.
- Country
- United States
- FDA Decision
- Deleted
- Decision Date
- 4/17/2023
- Days to Decision
- 208 days