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FDA 510(k), K192207, Trevo NXT ProVue Retriever
FDA 510(k), K192207, Trevo NXT ProVue Retriever
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$149.00 USD
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510(K) Number: K192207
Device Name: Trevo NXT ProVue Retriever
Manufacturer: Stryker
Device Classification Name: neurovascular mechanical thrombectomy device for acute ischemic stroke treatment
Regulation Number: 882.5600
Classification Product Code: POL
Date Received: 08/14/2019
Decision Date: 11/22/2019
Regulation Medical Specialty: Neurology
Device Name: Trevo NXT ProVue Retriever
Manufacturer: Stryker
Device Classification Name: neurovascular mechanical thrombectomy device for acute ischemic stroke treatment
Regulation Number: 882.5600
Classification Product Code: POL
Date Received: 08/14/2019
Decision Date: 11/22/2019
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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