MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-05-04 for MALIS 80-1531 manufactured by Symmetry Surgical Inc..
[74487269]
Patient Sequence No: 1, Text Type: N, H10
[74487270]
Surgeon was using the malis right angle ball tip nerve hook and the ball tip broke off during c5-7 anterior cervical discectomy fusion.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6546018 |
| MDR Report Key | 6546018 |
| Date Received | 2017-05-04 |
| Date of Report | 2017-04-11 |
| Date of Event | 2017-03-30 |
| Report Date | 2017-04-11 |
| Date Reported to FDA | 2017-04-11 |
| Date Reported to Mfgr | 2017-04-11 |
| Date Added to Maude | 2017-05-04 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | MALIS |
| Generic Name | HOOK, SURGICAL, GENERAL & PLASTIC SURGERY |
| Product Code | GDG |
| Date Received | 2017-05-04 |
| Model Number | 80-1531 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SYMMETRY SURGICAL INC. |
| Manufacturer Address | 3034 OWEN DR. ANTIOCH TN 37013 US 37013 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-05-04 |