MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2001-06-06 for FREEHAND SYSTEM IMPLANTABLE RECEIVER STIMULATOR 1060-1 NA manufactured by Neurocontrol Corporation.
[16396840]
Patient was implanted with the freehand system hand grasp neuroprosthesis in 1998. In 2001, the user facility reported the patient's hand was not responding to the stimulation from the implantable receiver stimulator (irs). Surface potential mapping was performed and malfunction of the irs was confirmed. No pt injury was involved. However, the patient has elected to undergo replacement surgery.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1530440-2001-00017 |
| MDR Report Key | 336688 |
| Report Source | 06,07 |
| Date Received | 2001-06-06 |
| Date of Report | 2001-05-07 |
| Date of Event | 2001-05-07 |
| Date Mfgr Received | 2001-05-07 |
| Device Manufacturer Date | 1997-08-01 |
| Date Added to Maude | 2001-06-12 |
| 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 |
| Reporter Occupation | OCCUPATIONAL THERAPIST |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 0 |
| Manufacturer Contact | PAMELA THOMAS |
| Manufacturer Street | 8333 ROCKSIDE ROAD |
| Manufacturer City | VALLEY VIEW OH 44125 |
| Manufacturer Country | US |
| Manufacturer Postal | 44125 |
| Manufacturer Phone | 2169120101 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | FREEHAND SYSTEM IMPLANTABLE RECEIVER STIMULATOR |
| Generic Name | IMPLANTABLE HAND GRASP NEUROPROSTHESIS |
| Product Code | GZC |
| Date Received | 2001-06-06 |
| Model Number | 1060-1 |
| Catalog Number | NA |
| Lot Number | NA |
| ID Number | NA |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Implant Flag | Y |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 325988 |
| Manufacturer | NEUROCONTROL CORPORATION |
| Manufacturer Address | 8333 ROCKSIDE ROAD VALLEY VIEW OH 44125 US |
| Baseline Brand Name | FREEHAND SYSTEM |
| Baseline Generic Name | NEUROMUSCULAR STIMULATOR IMPLANT |
| Baseline Model No | 1060-1 |
| Baseline Catalog No | NA |
| Baseline ID | NA |
| Baseline Device Family | FREEHAND SYSTEM IMPLANTABLE RECEIVER STIMULATOR |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | Y |
| Premarket Approval | P9500 |
| Baseline 510K PMN | N |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2001-06-06 |