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FDA 510(k), K210021, Axon Therapy
FDA 510(k), K210021, Axon Therapy
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$149.00 USD
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510(K) Number: K210021
Device Name: Axon Therapy
Manufacturer: NeuraLace Medical, Inc.
Device Classification Name: Electromagnetic Stimulator, Pain Relief
Regulation Number: 882.5890
Classification Product Code: QPL
Date Received: 01/04/2021
Decision Date: 06/11/2021
Regulation Medical Specialty: Neurology
Device Name: Axon Therapy
Manufacturer: NeuraLace Medical, Inc.
Device Classification Name: Electromagnetic Stimulator, Pain Relief
Regulation Number: 882.5890
Classification Product Code: QPL
Date Received: 01/04/2021
Decision Date: 06/11/2021
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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