MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-09-14 for COLLECT.NO.QAS SPINE SPECIALITIES AE-QAS-SP45 manufactured by Aesculap Implant Systems.
[86634107]
Manufacturing site evaluation: evaluation on-going. Device not returned.
Patient Sequence No: 1, Text Type: N, H10
[86634108]
Country of complaint: usa. Activ-l placed in (b)(6) 2016 progressively migrated anteriorly. Postop device failure. Surgeon opted for posterior fixation and observation. Implant originally placed (b)(6) 2016 lumbar tdr (total disc replacement). Intervention: posterior pedicle screw fixation (b)(6) 2017. Additional intervention needed a posterior pedicle screw fixation.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9610612-2017-00464 |
| MDR Report Key | 6865556 |
| Date Received | 2017-09-14 |
| Date of Report | 2018-08-06 |
| Date Facility Aware | 2017-09-13 |
| Date Mfgr Received | 2017-09-22 |
| Date Added to Maude | 2017-09-14 |
| 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 | MS. NICOLE BROYLES |
| Manufacturer Street | 615 LAMBERT POINTE DRIVE |
| Manufacturer City | HAZELWOOD MO 63042 |
| Manufacturer Country | US |
| Manufacturer Postal | 63042 |
| Manufacturer G1 | AESCULAP AG |
| Manufacturer Street | PO BOX 40 |
| Manufacturer City | TUTTLINGEN, 78501 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 78501 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | COLLECT.NO.QAS SPINE SPECIALITIES |
| Generic Name | SPINAL SPECIALITIES AND OTHERS |
| Product Code | JDN |
| Date Received | 2017-09-14 |
| Model Number | AE-QAS-SP45 |
| Catalog Number | AE-QAS-SP45 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | AESCULAP IMPLANT SYSTEMS |
| Manufacturer Address | PO BOX 40 TUTTLINGEN, 78501 GM 78501 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2017-09-14 |