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Relievant Medsystems

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222281Intracept Intraosseous Nerve Ablation SystemOctober 26, 2022
K213836Intracept Intraosseous Nerve Ablation SystemMarch 11, 2022
K190504Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation SysteMay 3, 2019
K180369Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)September 14, 2018
K171143Relievant Medsystems RF GeneratorAugust 18, 2017
K170827INTRACEPT Intraosseous Nerve Ablation SystemAugust 9, 2017
K153272INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument SetJuly 9, 2016
K100641INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND EASY ACCESS INSTRUMENT SET, MODEL FG0018 (PROBE), FG0036 (IMarch 30, 2010
K083856INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026January 22, 2009
K070443INTRACEPT BI-POLAR RF PROBE, MODEL 04814October 5, 2007