4.0MM TI CORTEX EXPANSIONHEAD SCREW SELF-DRILLING 16MM Adverse Event — Malfunction (MDR 8030965-2020-03125)
4.0MM TI CORTEX EXPANSIONHEAD SCREW SELF-DRILLING 16MM Adverse Event — Malfunction (MDR 8030965-2020-03125) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 4.0MM TI CORTEX EXPANSIONHEAD SCREW SELF-DRILLING 16MM; Generic name: APPLIANCE,FIXATION,SPINAL INTERVERTEBRAL BODY; Manufa
| Device | 4.0MM TI CORTEX EXPANSIONHEAD SCREW SELF-DRILLING 16MM |
|---|---|
| Generic name | APPLIANCE,FIXATION,SPINAL INTERVERTEBRAL BODY |
| Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
| Report number | 8030965-2020-03125 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | THE DEVICE HAS BEEN RECEIVED, THE INVESTIGATION IS IN PROGRESS, NO CONCLUSION COULD BE DRAWN AT THE TIME OF FILING THIS REPORT. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. |
| Source | openFDA MAUDE (device adverse events) |
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