MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-17 for SPECTRANETICS CORONARY LASER ATHERECTOMY CATHETER 114-009 manufactured by Spectranetics.
[92465428]
Patient Sequence No: 1, Text Type: N, H10
[92465429]
It was reported that during a coronary vascular intervention procedure to treat a thrombotic lesion in the left anterior descending (lad) vessel, a perforation occurred. Reportedly, a lesion in lad #6 was initially treated successfully with the elca device. Upon visualizing the area via angiography, a thrombotic lesion was identified in lad #7. This lesion was then treated in the same way. Angiography then showed a perforation. The perforation was successfully treated with perfusion balloon catheter. The patient was transferred to icu and outcome was good.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1721279-2017-00265 |
| MDR Report Key | 7043298 |
| Date Received | 2017-11-17 |
| Date of Report | 2017-10-25 |
| Date of Event | 2017-10-22 |
| Date Mfgr Received | 2017-10-25 |
| Device Manufacturer Date | 2017-06-05 |
| Date Added to Maude | 2017-11-17 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. NICK MCNABB |
| Manufacturer Street | 9965 FEDERAL DRIVE |
| Manufacturer City | COLORADO SPRINGS CO 80921 |
| Manufacturer Country | US |
| Manufacturer Postal | 80921 |
| Manufacturer Phone | 719447-257 |
| Manufacturer G1 | SPECTRANETICS |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | SPECTRANETICS CORONARY LASER ATHERECTOMY CATHETER |
| Generic Name | ELCA |
| Product Code | LPC |
| Date Received | 2017-11-17 |
| Model Number | 114-009 |
| Catalog Number | 114-009 |
| Lot Number | FTT17F05A |
| ID Number | NI |
| Device Expiration Date | 2019-06-07 |
| Operator | PHYSICIAN |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SPECTRANETICS |
| Manufacturer Address | 9965 FEDERAL DRIVE COLORADO SPRINGS CO 80921 US 80921 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2017-11-17 |