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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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85 records meeting your search criteria returned- Product Code: NJE Patient Problem: Transient Ischemic Attack Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
STRYKER NEUROVASCULAR-CALIF UNKNOWN_NEUROVASCULAR_PRODUCT 03/02/2017
STRYKER NEUROVASCULAR-CALIF UNKNOWN_NEUROVASCULAR_PRODUCT 03/02/2017
STRYKER NEUROVASCULAR-CALIF F/G WINGSPAN STENT SYSTEM 3.0 X 9MM 12/13/2016
CODMAN AND SHURTLEFF, INC ENTERPRISE VASCULAR RECONSTRUCTION DEVIC 11/11/2016
STRYKER NEUROVASCULAR CORK NEUROFORM 3 EZ- 4.5 X 20MM 09/23/2016
STRYKER NEUROVASCULAR-CALIF F/G WINGSPAN STENT SYSTEM 2.5 X 9MM 07/08/2016
STRYKER NEUROVASCULAR CORK NEUROFORM 3 EZ- 4.0 X 15MM 06/16/2016
CODMAN AND SHURTLEFF, INC ENTERPRISE VASCULAR RECONSTRUCTION DEVIC 06/07/2016
STRYKER NEUROVASCULAR-CALIF UNKNOWN_NEUROVASCULAR_PRODUCT 05/25/2016
STRYKER NEUROVASCULAR-CALIF UNKNOWN_NEUROVASCULAR_PRODUCT 05/25/2016
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