MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-22 for CD HORIZON SPINAL SYSTEM 1556300500 manufactured by Warsaw Orthopedics.
[184452885]
This part is not approved for use in the united states; however a like device catalog # 1556200500, 510k # k131321 and udi # (b)(4) was cleared in the united states. Product was not returned to the manufacturer for evaluation. Therefore, we are unable to determine the definitive cause of the reported event. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[184452886]
It was reported that the patient presented with spinal kyphoscoliosis; and underwent fixation surgery at t8-s2ai. On an unknown date, post-op, the rod implanted on the left broke at l3-l4. Along with this rod, the screw broke at s2ai and the rod on the right broke at l4-l5. Hence, a revision surgery was performed, in which the broken rods were completely explanted. Rod reinforcement was also performed. The broken screw could not be removed and was left implanted in the patient? S body. Reportedly, the rod had not broken until last december. According to the healthcare professional, since the broken surface had not shown metallosis, it seemed the breakage was not due to metallic fatigue.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1030489-2020-00354 |
| MDR Report Key | 9863853 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2020-03-22 |
| Date of Report | 2020-03-22 |
| Date Mfgr Received | 2020-02-26 |
| Device Manufacturer Date | 2016-02-26 |
| Date Added to Maude | 2020-03-22 |
| 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 | STACIE ZIEMBA |
| Manufacturer Street | 1800 PYRAMID PLACE |
| Manufacturer City | MEMPHIS TN 38132 |
| Manufacturer Country | US |
| Manufacturer Postal | 38132 |
| Manufacturer Phone | 9013963133 |
| Manufacturer G1 | WARSAW ORTHOPEDICS |
| Manufacturer Street | 2500 SILVEUS CROSSING |
| Manufacturer City | WARSAW IN 46582 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 46582 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CD HORIZON SPINAL SYSTEM |
| Product Code | KWP |
| Date Received | 2020-03-22 |
| Model Number | NA |
| Catalog Number | 1556300500 |
| Lot Number | 0451853W |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | WARSAW ORTHOPEDICS |
| Manufacturer Address | 2500 SILVEUS CROSSING WARSAW IN 46582 US 46582 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-03-22 |