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 2019-10-30 for TI VECTRA-ONE PLATE 2 LEVEL/36MM 04.613.186 manufactured by Wrights Lane Synthes Usa Products Llc.
Report Number | 2939274-2019-61827 |
MDR Report Key | 9256041 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-10-30 |
Date of Report | 2019-10-14 |
Date of Event | 2019-10-14 |
Date Mfgr Received | 2019-11-06 |
Device Manufacturer Date | 2016-05-11 |
Date Added to Maude | 2019-10-30 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KARA DITTY-BOVARD |
Manufacturer Street | 1302 WRIGHTS LANE EAST |
Manufacturer City | WEST CHESTER PA 19380 |
Manufacturer Country | US |
Manufacturer Postal | 19380 |
Manufacturer Phone | 6103142063 |
Manufacturer G1 | WERK MEZZOVICO (CH) |
Manufacturer Street | VIA CAVAZZ 5 |
Manufacturer City | MEZZOVICO 6805 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 6805 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TI VECTRA-ONE PLATE 2 LEVEL/36MM |
Generic Name | INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL |
Product Code | ODP |
Date Received | 2019-10-30 |
Catalog Number | 04.613.186 |
Lot Number | 9938529 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | WRIGHTS LANE SYNTHES USA PRODUCTS LLC |
Manufacturer Address | 1302 WRIGHTS LANE EAST WEST CHESTER PA 19380 US 19380 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-30 |