MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 02,05,07 report with the FDA on 2013-02-27 for SPINE manufactured by Synthes.
[3172291]
Patient 1, it was reported that the spacer as moved. There is no additional information available.
Patient Sequence No: 1, Text Type: D, B5
[10507096]
Without lot number the device history records review could not be completed. The investigation could not be completed; no conclusion could be drawn, as no product was received. Placeholder.
Patient Sequence No: 1, Text Type: N, H10
[28836709]
Device was used for treatment, not diagnosis. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[28836710]
This is report 1 of 1 for complaint (b)(4).
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2520274-2013-01213 |
MDR Report Key | 2981356 |
Report Source | 02,05,07 |
Date Received | 2013-02-27 |
Date of Report | 2011-07-25 |
Date Mfgr Received | 2014-01-28 |
Date Added to Maude | 2013-05-07 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | P NEAL |
Manufacturer Street | 1302 WRIGHTS LANE EAST |
Manufacturer City | WEST CHESTER PA 19380 |
Manufacturer Country | US |
Manufacturer Postal | 19380 |
Manufacturer Phone | 8006207025 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SPINE |
Product Code | LYQ |
Date Received | 2013-02-27 |
Catalog Number | SPINE |
Operator | PHYSICIAN |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SYNTHES |
Manufacturer Address | 1302 WRIGHTS LANE EAST WEST CHESTER PA 19380 19380 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2013-02-27 |