FDA 510(k) Applications Submitted by Alex DiNello

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180369	02/12/2018	Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)	Relievant Medsystems
K190504	03/01/2019	Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF Generator	Relievant Medsystems
K170827	03/20/2017	INTRACEPT Intraosseous Nerve Ablation System	Relievant Medsystems
K171143	04/18/2017	Relievant Medsystems RF Generator	Relievant Medsystems