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 2020-03-26 for SUPERION INDIRECT DECOMPRESSION SYSTEM 101-9816 manufactured by Vertiflex Inc..
[185892974]
It was reported that the patient was explanted due to the spacer being displaced. The spacer was kept by the medical facility.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3006630150-2020-01462 |
MDR Report Key | 9884827 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-26 |
Date of Report | 2020-03-26 |
Date of Event | 2020-01-27 |
Date Mfgr Received | 2020-02-26 |
Date Added to Maude | 2020-03-26 |
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 | TALAR TAHMASIAN |
Manufacturer Street | 25155 RYE CANYON LOOP |
Manufacturer City | VALENCIA CA 91355 |
Manufacturer Country | US |
Manufacturer Postal | 91355 |
Manufacturer Phone | 6619494863 |
Manufacturer G1 | VERTIFLEX INC |
Manufacturer City | CARLSBAD CA 92010 |
Manufacturer Country | US |
Manufacturer Postal Code | 92010 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SUPERION INDIRECT DECOMPRESSION SYSTEM |
Generic Name | PROSTHESIS, SPINOUS PROCESS SPACER/PLATE |
Product Code | NQO |
Date Received | 2020-03-26 |
Model Number | 101-9816 |
Catalog Number | 101-9816 |
Lot Number | 800223 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | VERTIFLEX INC. |
Manufacturer Address | 2714 LOKER AVE. WEST SUITE 100 CARLSBAD CA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-26 |