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FDA 510(k), K162999, V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System
FDA 510(k), K162999, V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System
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510(K) Number: K162999
Device Name: V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System
Manufacturer: MICROVENTION, INC
Device Classification Name: device, neurovascular embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 10/28/2016
Decision Date: 03/29/2017
Regulation Medical Specialty: Neurology
Device Name: V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System
Manufacturer: MICROVENTION, INC
Device Classification Name: device, neurovascular embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 10/28/2016
Decision Date: 03/29/2017
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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