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FDA 510(k), K152178, StimQ Peripheral Nerve Stimulator (PNS) System
FDA 510(k), K152178, StimQ Peripheral Nerve Stimulator (PNS) System
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510(K) Number: K152178
Device Name: StimQ Peripheral Nerve Stimulator (PNS) System
Manufacturer: STIMQ LLC
Device Classification Name: stimulator, peripheral nerve, implanted (pain relief)
Regulation Number: 882.5870
Classification Product Code: GZF
Date Received: 08/04/2015
Decision Date: 03/11/2016
Regulation Medical Specialty: Neurology
Device Name: StimQ Peripheral Nerve Stimulator (PNS) System
Manufacturer: STIMQ LLC
Device Classification Name: stimulator, peripheral nerve, implanted (pain relief)
Regulation Number: 882.5870
Classification Product Code: GZF
Date Received: 08/04/2015
Decision Date: 03/11/2016
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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