MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-12-13 for VLIFT CAGE DIAM 18 X 32MM 48291832 manufactured by Stryker Spine-us.
[174707689]
Other text : status and location of the device are currently unknown.
Patient Sequence No: 1, Text Type: N, H10
[174707690]
It was reported that a vlift cage in l3 migrated post-operatively. Revision surgery was performed during which a new cage was placed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0009617544-2019-00137 |
| MDR Report Key | 9466705 |
| Report Source | COMPANY REPRESENTATIVE |
| Date Received | 2019-12-13 |
| Date of Report | 2020-03-24 |
| Date of Event | 2019-12-03 |
| Date Mfgr Received | 2020-02-27 |
| Device Manufacturer Date | 2019-03-13 |
| Date Added to Maude | 2019-12-13 |
| 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. RITA KARAN |
| Manufacturer Street | 2 PEARL COURT |
| Manufacturer City | ALLENDALE NJ 07401 |
| Manufacturer Country | US |
| Manufacturer Postal | 07401 |
| Manufacturer Phone | 2017608000 |
| Manufacturer G1 | STRYKER SPINE-FRANCE |
| Manufacturer Street | ZONE INDUSTRIELLE DE MARTICOT |
| Manufacturer City | CESTAS 33610 |
| Manufacturer Country | FR |
| Manufacturer Postal Code | 33610 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | VLIFT CAGE DIAM 18 X 32MM |
| Generic Name | SPINAL VERTEBRAL BODY REPLACEMENT |
| Product Code | MQP |
| Date Received | 2019-12-13 |
| Model Number | 48291832 |
| Catalog Number | 48291832 |
| Lot Number | 191685 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER SPINE-US |
| Manufacturer Address | 2 PEARL COURT ALLENDALE NJ 07401 US 07401 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2019-12-13 |