MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2019-03-12 for UNKNOWN RESPONSE PEDICLE SCREW N/A manufactured by Orthopediatrics, Inc.
[139825734]
Reference: (b)(4). Customer has not returned the device as it is still implanted. The investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10
[139825735]
It has been reported that following the placement of response spine construct, a screw broke in the pedicle. Attempts have been made and additional information on the reported event is unavailable at this time. No adverse events have been reported as a result of the malfunction.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3006460162-2019-00009 |
MDR Report Key | 8414468 |
Report Source | DISTRIBUTOR,HEALTH PROFESSION |
Date Received | 2019-03-12 |
Date of Report | 2019-03-12 |
Date of Event | 2019-02-11 |
Date Mfgr Received | 2019-02-11 |
Date Added to Maude | 2019-03-12 |
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 | LEIGH JESSOP |
Manufacturer Street | 2850 FRONTIER DRIVE |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal | 46582 |
Manufacturer Phone | 5142670872 |
Manufacturer G1 | ORTHOPEDIATRICS, INC |
Manufacturer Street | 2850 FRONTIER DRIVE |
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 | UNKNOWN RESPONSE PEDICLE SCREW |
Generic Name | PEDICLE SCREW SPINAL SYSTEM |
Product Code | OSH |
Date Received | 2019-03-12 |
Model Number | N/A |
Catalog Number | UNKNOWN |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ORTHOPEDIATRICS, INC |
Manufacturer Address | 2850 FRONTIER DRIVE WARSAW IN 46582 US 46582 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-03-12 |