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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
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