MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-03-11 for PIONEER STERNAL CABLE SYSTEM 400-425 N/A manufactured by Pioneer Surgical (d.b.a. Rti Surgical).
| Report Number | 1833824-2020-00018 |
| MDR Report Key | 9817343 |
| Report Source | OTHER |
| Date Received | 2020-03-11 |
| Date of Report | 2020-03-11 |
| Date of Event | 2019-04-15 |
| Date Mfgr Received | 2020-02-12 |
| Device Manufacturer Date | 2019-05-14 |
| Date Added to Maude | 2020-03-11 |
| 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 | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. DANIEL NELSON |
| Manufacturer Street | 375 RIVER PARK CIRCLE |
| Manufacturer City | MARQUETTE, MI |
| Manufacturer Country | US |
| Manufacturer Phone | 2264489 |
| Manufacturer G1 | PIONEER SURGICAL (D.B.A. RTI SURGICAL) |
| Manufacturer Street | 375 RIVER PARK CIRCLE |
| Manufacturer City | MARQUETTE, MI |
| Manufacturer Country | US |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PIONEER STERNAL CABLE SYSTEM |
| Generic Name | STERNAL FIXATION CABLE |
| Product Code | JDQ |
| Date Received | 2020-03-11 |
| Model Number | 400-425 |
| Catalog Number | N/A |
| Lot Number | 314215 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PIONEER SURGICAL (D.B.A. RTI SURGICAL) |
| Manufacturer Address | 375 RIVER PARK CIRCLE MARQUETTE, MI US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2020-03-11 |