MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2008-12-12 for LIFE INSTRUMENTS 713-9506-0 manufactured by .
[18833473]
Dr posterior lumbar interbody fusion case l5-s1 curette tip broke off during surgery. Multiple xrays shot through at surgery to check on placement of implants.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5009307 |
| MDR Report Key | 1272447 |
| Date Received | 2008-12-12 |
| Date of Report | 2008-11-18 |
| Date of Event | 2008-11-18 |
| Date Added to Maude | 2009-01-15 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | LIFE INSTRUMENTS |
| Generic Name | SPINAL CURETTE #6/0 STR |
| Product Code | HTF |
| Date Received | 2008-12-12 |
| Model Number | 713-9506-0 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2008-12-12 |