FDA 510(k) Applications Submitted by Relievant Medsystems, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K070443 02/15/2007 INTRACEPT BI-POLAR RF PROBE, MODEL 04814 RELIEVANT MEDSYSTEMS, INC.
K083856 12/24/2008 INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026 RELIEVANT MEDSYSTEMS, INC.
K213836 12/09/2021 Intracept Intraosseous Nerve Ablation System Relievant Medsystems, Inc.
K222281 07/29/2022 Intracept Intraosseous Nerve Ablation System Relievant Medsystems, Inc.


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