FDA Adverse Event Death Summary report: N

RESOLUTE INTEGRITY RX

MDR report key: 7964597 · Received October 15, 2018

Report

Report Number
9612164-2018-02737
Event Type
Death
Date Received
October 15, 2018
Date of Event
April 26, 2018
Report Date
October 15, 2018
Manufacturer
MEDTRONIC IRELAND
Product Code
NIQ
PMA / PMN Number
P110013
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

AGE/DATE OF BIRTH: AVERAGE AGE. SEX: MAJORITY GENDER. DATE OF EVENT: DATE OF PUBLICATION. PACLITAXEL-COATED BALLOON TREATMENT FOR FUNCTIONALLY NONSIGNIFICANT RESIDUAL CORONARY LESIONS AFTER BALLOON ANGIOPLASTY. AVAILABLE : HTTPS://DOI.ORG/10.1007/S10554-018-1351-Z. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED VIA JOURNAL THAT RESOLUTE INTEGRITY WERE INCLUDED IN A STUDY COMPARING THE EFFICACY OF PCB TREATMENT WITH STENT IMPLANT IN NEW LESIONS FOLLOWING SUCCESSFUL POBA. INCLUSION CRITERIA WERE THE PRESENCE OF A SINGLE NEW CORONARY LESION WITH A REFERENCE DIAMETER BETWEEN 2.5 AND 3.5MM, A LESION LENGTH <_ 24MM AND TIMI FLOW 3 FOLLOWING POBA. LESIONS TREATED INCLUDED LAD, LCX AND RCA. ADVERSE EVENTS REPORTED INCLUDED DEATH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
806377 RESOLUTE INTEGRITY RX STENT, CORONARY, DRUG-ELUTING NIQ MEDTRONIC IRELAND

Patients

Seq Age Sex Outcome Treatment
1 59 YR Death