MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1998-02-19 for DURAMER ADVANTIM POST STAB LSI TIBIAL INSERT 1890-3212 manufactured by Wright Medical Technology, Inc.
| Report Number | 1043534-1998-00022 |
| MDR Report Key | 150190 |
| Report Source | 06 |
| Date Received | 1998-02-19 |
| Date of Event | 1997-09-11 |
| Date Mfgr Received | 1998-01-22 |
| Device Manufacturer Date | 1994-08-01 |
| Date Added to Maude | 1998-02-24 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 0 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DURAMER ADVANTIM POST STAB LSI TIBIAL INSERT |
| Generic Name | KNEE COMPONENT |
| Product Code | KRP |
| Date Received | 1998-02-19 |
| Model Number | NA |
| Catalog Number | 1890-3212 |
| Lot Number | 084A005297 |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Implant Flag | Y |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 146342 |
| Manufacturer | WRIGHT MEDICAL TECHNOLOGY, INC |
| Manufacturer Address | 5677 AIRLINE RD ARLINGTON TN 38002 US |
| Baseline Brand Name | DURAMER ADVANTIM POST STAB LSI TIBIAL INSERT |
| Baseline Generic Name | KNEE COMPONENT |
| Baseline Catalog No | 1890-3212 |
| Baseline Device Family | K J 888.3560 |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | N |
| Baseline Preamendment | Y |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1998-02-19 |