MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 1999-04-07 for SINGLE VECTOR DISTRACTOR BODY-LEFT 487.963.311 manufactured by .
| Report Number | 2520274-1999-00020 |
| MDR Report Key | 218615 |
| Report Source | 05,06 |
| Date Received | 1999-04-07 |
| Date of Event | 1999-03-13 |
| Date Mfgr Received | 1999-03-12 |
| Date Added to Maude | 1999-04-15 |
| 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 | 0 |
| Event Location | 0 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SINGLE VECTOR DISTRACTOR BODY-LEFT |
| Generic Name | MANDIBLE DISTRACTOR |
| Product Code | MON |
| Date Received | 1999-04-07 |
| Model Number | NA |
| Catalog Number | 487.963.311 |
| Lot Number | NI |
| ID Number | NA |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 212021 |
| Baseline Brand Name | SINGLE VECTOR DISTRACTOR BODY/20MM/LEFT |
| Baseline Generic Name | MANDIBLE DISTRACTOR |
| Baseline Model No | NA |
| Baseline Catalog No | 487.963.311 |
| Baseline ID | NA |
| Baseline Device Family | MANDIBLE DISTRACTOR |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | Y |
| Premarket Notification | K962272 |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 1999-04-07 |