MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-17 for PEDICLE PROBE, LENKE CURVED (STAINLESS STEEL) 22SPT10 manufactured by Alphatec Spine Inc.
| Report Number | 2027467-2019-00044 |
| MDR Report Key | 9075980 |
| Date Received | 2019-09-17 |
| Date of Report | 2019-08-15 |
| Date of Event | 2019-08-15 |
| Date Mfgr Received | 2019-08-19 |
| Device Manufacturer Date | 2012-02-01 |
| Date Added to Maude | 2019-09-17 |
| 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 | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. RICHARD YOUNGER |
| Manufacturer Street | 5818 EL CAMINO REAL |
| Manufacturer City | CARLSBAD CA 92008 |
| Manufacturer Country | US |
| Manufacturer Postal | 92008 |
| Manufacturer Phone | 7604946842 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | PEDICLE PROBE, LENKE CURVED (STAINLESS STEEL) |
| Generic Name | HXB |
| Product Code | HXB |
| Date Received | 2019-09-17 |
| Returned To Mfg | 2019-08-22 |
| Model Number | 22SPT10 |
| Catalog Number | 22SPT10 |
| Lot Number | 6505607 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ALPHATEC SPINE INC |
| Manufacturer Address | 5818 EL CAMINO REAL CARLSBAD CA 92008 US 92008 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-09-17 |