MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 03,05 report with the FDA on 2010-08-06 for INFUSE BONE GRAFT UNK manufactured by Medtronic Sofamor Danek Usa, Inc..
[1570514]
It was reported that pts with a history of humeral nonunions were treated with rhbmp-2. After adequate bone preparation and reduction, locking plates were applied. Minimal contouring was needed. Six to eight cortices were used on either side on the nonunion site. In one pt, despite some bone formation, union had not occurred after one year. No infection was observed. Revision with the same technique was required and union was achieved ten months later.
Patient Sequence No: 1, Text Type: D, B5
[8683457]
Literature citation: crawford et al. Atrophic nonunion of humeral diaphysis treated with locking plate and recombinant bone morphogenetic protein: nine cases. The american journal of orthopedics, 2009; 38(11): 567-570. A review of the device history records is not possible without add'l device info. Neither the device nor imaging films were returned to the mfr for eval. Therefore, we are unable to determine the definitive cause of the reported event. (b)(4): pseudoarthrosis.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1030489-2010-01030 |
| MDR Report Key | 1793154 |
| Report Source | 03,05 |
| Date Received | 2010-08-06 |
| Date of Report | 2010-07-16 |
| Date of Event | 2009-11-01 |
| Date Mfgr Received | 2010-07-16 |
| Date Added to Maude | 2010-08-17 |
| 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 | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | CHAD ASHTON |
| Manufacturer Street | 1800 PYRAMID PLACE |
| Manufacturer City | MEMPHIS TN 38132 |
| Manufacturer Country | US |
| Manufacturer Postal | 38132 |
| Manufacturer Phone | 9013963133 |
| Manufacturer G1 | MEDTRONIC SOFAMOR DANEK USA, INC. |
| Manufacturer Street | 4340 SWINNEA RD |
| Manufacturer City | MEMPHIS TN 38118 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 38118 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | INFUSE BONE GRAFT |
| Generic Name | INFUSE BONE GRAFT |
| Product Code | MPW |
| Date Received | 2010-08-06 |
| Model Number | NA |
| Catalog Number | UNK |
| Lot Number | UNK |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | NA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC SOFAMOR DANEK USA, INC. |
| Manufacturer Address | 4340 SWINNEA RD MEMPHIS TN 38118 US 38118 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2010-08-06 |