STELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON A35SX040040135

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,study report with the FDA on 2020-03-19 for STELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON A35SX040040135 manufactured by Spectranetics.

Event Text Entries

[184147189] The patient's cause of death was unrelated to the study device or procedure. This is being reported as a follow-up to the clinical registry. Cross reference mfr report numbers: 3009784280-2020-00070, 3009784280-2020-00071. Patient information regarding relevant tests/laboratory data is unknown. This information was not available from the facility. Report source: foreign- (b)(6)/ study name: (b)(6): patient id # (b)(6). Pma number is not applicable. The device is a commercial product with a ce mark that was used as part of a clinical registry. During the index procedure, the product worked as intended and the device was discarded, thus no product evaluation was required. Per the ifu, death is listed as a potential complications/adverse events.
Patient Sequence No: 1, Text Type: N, H10


[184147190] It was reported through a clinical registry that during the index procedure on (b)(6) 2018, two stellarex catheters were used to treat the target lesions of the right infrapopliteal, proximal and distal tibialis anterior. Approximately 12 months post index procedure, the patient expired due to renal failure on (b)(6) 2019.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009784280-2020-00070
MDR Report Key9855699
Report SourceFOREIGN,STUDY
Date Received2020-03-19
Date of Report2020-03-04
Date of Event2018-12-02
Report Date2005-01-01
Date Reported to FDA2005-01-01
Date Reported to Mfgr2005-01-10
Date Mfgr Received2020-03-04
Date Added to Maude2020-03-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. ANA TAN
Manufacturer Street5055 BRANDIN COURT
Manufacturer CityFREMONT CA 94538
Manufacturer CountryUS
Manufacturer Postal94538
Manufacturer Phone510933-798
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 Received2020-03-19
Model NumberA35SX040040135
Catalog NumberA35SX040040135
Lot NumberFCU17M05A
Device Expiration Date2019-12-19
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
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 Received2020-03-19
Device Sequence No101
Device Event Key0
ManufacturerSPECTRANETICS


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-19

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