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 2017-04-21 for KYPHON EXPRESS BONE BIOPSY DEVICE F07A manufactured by Medtronic Sofamor Danek Usa, Inc.
[73333042]
Neither the device nor films of applicable imaging studies were returned to the manufacturer for evaluation. Therefore, we are unable to determine the definitive cause of the reported event.
Patient Sequence No: 1, Text Type: N, H10
[73333043]
Pre-operative diagnosis: osteoporosis procedure: bone biopsy level: l3 it was reported that during surgery, the tip of the device broke while performing bone biopsy. The tip remained on the right side of the vertebral body. No patient complications were reported as a result of the event.
Patient Sequence No: 1, Text Type: D, B5
[100715871]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1030489-2017-00960 |
| MDR Report Key | 6510536 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2017-04-21 |
| Date of Report | 2017-10-17 |
| Date of Event | 2017-03-28 |
| Date Mfgr Received | 2017-03-28 |
| Date Added to Maude | 2017-04-21 |
| 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 | GREG ANGLIN |
| Manufacturer Street | 1800 PYRAMID PLACE |
| Manufacturer City | MEMPHIS TN 38132 |
| Manufacturer Country | US |
| Manufacturer Postal | 38132 |
| Manufacturer Phone | 9013963133 |
| Manufacturer G1 | MEDTRONIC SOFAMOR DANEK USA, INC |
| Manufacturer Street | 4340 SWINEA RD |
| Manufacturer City | MEMPHIS TN 38118 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 38118 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | KYPHON EXPRESS BONE BIOPSY DEVICE |
| Generic Name | DEVICE, PERCUTANEOUS, BIOPSY |
| Product Code | MJG |
| Date Received | 2017-04-21 |
| Model Number | NA |
| Catalog Number | F07A |
| Lot Number | WI398406 |
| Device Expiration Date | 2017-06-15 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC SOFAMOR DANEK USA, INC |
| Manufacturer Address | 4340 SWINEA RD MEMPHIS TN 38118 US 38118 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-04-21 |