MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1998-10-15 for SILVER OSTEOTOME LEFT RH1462-002 manufactured by Allegiance Healthcare Corp..
[119084]
Left osteotome broke leaving 3mmx5mm fragment embedded in the pt's maxilla bone.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1423507-1998-00314 |
| MDR Report Key | 191945 |
| Report Source | 05 |
| Date Received | 1998-10-15 |
| Date of Report | 1998-10-15 |
| Date Mfgr Received | 1998-09-18 |
| Date Added to Maude | 1998-10-19 |
| 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 | 3 |
| Event Location | 0 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SILVER OSTEOTOME LEFT |
| Generic Name | INSTRUMENT |
| Product Code | GFI |
| Date Received | 1998-10-15 |
| Model Number | RH1462-002 |
| Catalog Number | RH1462-002 |
| Lot Number | * |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 186517 |
| Manufacturer | ALLEGIANCE HEALTHCARE CORP. |
| Manufacturer Address | 1500 WAUKEGAN RD. MCGAW PARK IL 60085 US |
| Baseline Brand Name | SILVER OSTEOTOME LEFT |
| Baseline Generic Name | INSTRUMENT |
| Baseline Model No | RH1462-002 |
| Baseline Catalog No | RH1462-002 |
| Baseline ID | NA |
| Baseline Device Family | INSTRUMENT |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | N |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | Y |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1998-10-15 |