FDA Adverse Event Death Summary report: N

DRIVER RX

MDR report key: 8644238 · Received May 27, 2019

Report

Report Number
9612164-2019-01996
Event Type
Death
Date Received
May 27, 2019
Date of Event
January 29, 2019
Report Date
May 27, 2019
Manufacturer
MEDTRONIC IRELAND
Product Code
MAF
PMA / PMN Number
P030009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

JOURNAL ARTICLE: PERIPROCEDURAL AND LONG-TERM OUTCOMES OF STENT IMPLANTATION FOR DE NOVO SUBCLAVIAN ARTERY DISEASE. DOI: 10.1177/1538574418824444. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

THE PURPOSE OF THE CURRENT STUDY WAS TO INVESTIGATE THE PERIPROCEDURAL AND LONG-TERM OUTCOMES OF STENT IMPLANTATION FOR DE NOVO SUBCLAVIAN ARTERY (SCA) DISEASE. PATIENTS WITH DE NOVO SCA LESIONS WHO UNDERWENT EVT PROCEDURES WERE INCLUDED IN THE ANALYSES OF PERIPROCEDURAL OUTCOMES. ASSURANT COBALT STENTS, DRIVER BARE METAL STENTS AND RESOLUTE INTEGRITY DRUG ELUTING STENTS WERE AMONG THE STENTS IMPLANTED. CLINICAL OUTCOMES REPORTED INCLUDED STENOSIS, RESTENOSIS, OCCLUSION, RE INTERVENTION OF THE TARGET VESSEL, DISTAL EMBOLISM, DISSECTION, PSEUDOANEURYSM AT ACCESS SITES, HEMATOMA AT ACCESS SITES, DEATH AND STROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
436707 DRIVER RX STENT, CORONARY MAF MEDTRONIC IRELAND UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 71 YR Death