MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-04-05 for COCHLEAR? VISTAFIX? VXA300 ABUTMENT 3.5MM 92994 manufactured by Cochlear Bone Anchored Solutions Ab.
[71824204]
This report is submitted on april 06, 2017. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[71824205]
Per the clinic, the patient experienced skin overgrowth and a possible infection at implant site. Subsequently, the patient was treated with antibiotics (date and type not reported) and patient was placed under general anesthesia to replace abutment.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6000034-2017-00622 |
| MDR Report Key | 6462740 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2017-04-05 |
| Date of Report | 2017-03-17 |
| Date Mfgr Received | 2017-03-17 |
| Date Added to Maude | 2017-04-05 |
| 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 | MS. KRISTEL KOHNE |
| Manufacturer Street | 1 UNIVERSITY AVENUE |
| Manufacturer City | MACQUARIE UNIVERSITY, NSW 2109, |
| Manufacturer Country | AS |
| Manufacturer Postal | 2109, |
| Manufacturer Phone | 94286555 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COCHLEAR? VISTAFIX? VXA300 ABUTMENT 3.5MM |
| Generic Name | COCHLEAR BAHA CONNECT SYSTEM |
| Product Code | FZE |
| Date Received | 2017-04-05 |
| Model Number | 92994 |
| Catalog Number | 92994 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COCHLEAR BONE ANCHORED SOLUTIONS AB |
| Manufacturer Address | KONSTRUKTIONSV?GEN 14 PO BOX 82 M?LNLYCKE, 435 22 SW 435 22 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2017-04-05 |