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FDA 510(k), K213836, Intracept Intraosseous Nerve Ablation System
FDA 510(k), K213836, Intracept Intraosseous Nerve Ablation System
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$149.00 USD
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$149.00 USD
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510(K) Number: K213836
Device Name: Intracept Intraosseous Nerve Ablation System
Manufacturer: Relievant Medsystems, Inc.
Device Classification Name: Probe, Radiofrequency Lesion
Regulation Number: 882.4725
Classification Product Code: GXI
Date Received: 12/09/2021
Decision Date: 03/11/2022
Regulation Medical Specialty: Neurology
Device Name: Intracept Intraosseous Nerve Ablation System
Manufacturer: Relievant Medsystems, Inc.
Device Classification Name: Probe, Radiofrequency Lesion
Regulation Number: 882.4725
Classification Product Code: GXI
Date Received: 12/09/2021
Decision Date: 03/11/2022
Regulation Medical Specialty: Neurology
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