MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2003-05-16 for KNIFELIGHT 3300-001-000 NA manufactured by Stryker Instruments.
[18821278]
It is alleged that a nerve in the right wrist of pt was cut during surgery. Pt has an alleged contracture and cannot move 2 fingers of the right palm.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2648666-2003-20002 |
| MDR Report Key | 461035 |
| Report Source | 01,07 |
| Date Received | 2003-05-16 |
| Date of Report | 2003-04-17 |
| Date of Event | 2003-04-17 |
| Report Date | 2003-04-17 |
| Date Mfgr Received | 2003-04-17 |
| Date Added to Maude | 2003-05-22 |
| 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 |
| Manufacturer Street | 4100 E MILHAM AVE |
| Manufacturer City | KALAMAZOO MI 49001 |
| Manufacturer Country | US |
| Manufacturer Postal | 49001 |
| Manufacturer Phone | 2693237700 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | KNIFELIGHT |
| Generic Name | KNIFE, SURGICAL |
| Product Code | EMF |
| Date Received | 2003-05-16 |
| Model Number | 3300-001-000 |
| Catalog Number | NA |
| Lot Number | NA |
| ID Number | NA |
| Device Availability | * |
| Device Age | UNKNOWN |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | U |
| Device Sequence No | 1 |
| Device Event Key | 449977 |
| Manufacturer | STRYKER INSTRUMENTS |
| Manufacturer Address | 4100 E MILHAM AVE KALAMAZOO MI 49001 US |
| Baseline Brand Name | KNIFELIGHT |
| Baseline Generic Name | KNIFE, SURGICAL LAMP, SURGICAL |
| Baseline Model No | 3300-001-000 |
| Baseline Catalog No | NA |
| Baseline ID | 3300-001-000 |
| Baseline Device Family | KNIFELIGHT |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | Y |
| Premarket Notification | K961122 |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2003-05-16 |