FDA Adverse Event Injury Summary report: N

MULTI-LINK RX VISION CORONARY STENT SYSTEM

MDR report key: 1040307 · Received April 30, 2008

Report

Report Number
2024168-2008-00361
Event Type
Injury
Date Received
April 30, 2008
Date of Event
March 27, 2008
Report Date
March 31, 2008
Manufacturer
ABBOTT VASCULAR-CARDIAC THERAPIES
Product Code
MAF
PMA / PMN Number
PO20047
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
PHYSICIAN

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MULTI-LINK RX VISION CORONARY STENT SYSTEM 74MAF MAF ABBOTT VASCULAR-CARDIAC THERAPIES NA 7112132

Patients

Seq Age Sex Outcome Treatment
1 71 YR Hospitalization| R