STELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON AB35SX060040135

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-31 for STELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON AB35SX060040135 manufactured by Spectranetics.

MAUDE Entry Details

Report Number3009784280-2020-00094
MDR Report Key9906201
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-31
Date of Report2020-03-04
Date of Event2020-02-11
Report Date2005-01-01
Date Reported to FDA2005-01-01
Date Reported to Mfgr2005-01-10
Date Mfgr Received2020-03-04
Date Added to Maude2020-03-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. FLORIE CAZEM
Manufacturer Street5055 BRANDIN COURT
Manufacturer CityFREMONT CA 94538
Manufacturer CountryUS
Manufacturer Postal94538
Manufacturer Phone510933-792
Manufacturer G1SPECTRANETICS
Manufacturer Street6531 DUMBARTON CIRCLE
Manufacturer CityFREMONT CA 94555
Manufacturer CountryUS
Manufacturer Postal Code94555
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Sequence Number: 1

Brand NameSTELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON
Generic NameDCB PTA CATHETER
Product CodeONU
Date Received2020-03-31
Returned To Mfg2020-03-27
Model NumberAB35SX060040135
Catalog NumberAB35SX060040135
Lot NumberFHT19A30A
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Sequence No1
Device Event Key0
ManufacturerSPECTRANETICS
Manufacturer Address6531 DUMBARTON CIRCLE FREMONT CA 94555 US 94555

Device Sequence Number: 101

Brand NamePACLITAXEL, 2 ?G/MM2
Product Code---
Date Received2020-03-31
Device Sequence No101
Device Event Key0
ManufacturerSPECTRANETICS


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-31

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.