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Relievant Medsystems, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2022-10-26
TypeNumberDevice NameCodeDateActions
510(k) K222281 Intracept Intraosseous Nerve Ablation SystemGXI2022-10-26 View
510(k) K213836 Intracept Intraosseous Nerve Ablation SystemGXI2022-03-11 View
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