MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-14 for UNKNOWN_K2M_PRODUCT UNK_SPE manufactured by K2m, Inc..
[183769010]
Return status of the device is unknown.
Patient Sequence No: 1, Text Type: N, H10
[183769011]
Stryker representative reported that the placement of an unknown illiac screw was not 'optimal' post-operatively. Revision surgery has occurred.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3004774118-2020-00029 |
MDR Report Key | 9832855 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-14 |
Date of Report | 2020-03-13 |
Date of Event | 2020-02-12 |
Date Mfgr Received | 2020-02-12 |
Date Added to Maude | 2020-03-14 |
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 | MR. RITA KARAN |
Manufacturer Street | 2 PEARL COURT |
Manufacturer City | ALLENDALE NJ 07401 |
Manufacturer Country | US |
Manufacturer Postal | 07401 |
Manufacturer Phone | 2017608000 |
Manufacturer G1 | K2M, INC. |
Manufacturer Street | 600 HOPE PARKWAY SE |
Manufacturer City | LEESBURG VA 20175 |
Manufacturer Country | US |
Manufacturer Postal Code | 20175 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNKNOWN_K2M_PRODUCT |
Generic Name | THORACOLUMBOSACRAL PEDICLE SCREW SYSTEM |
Product Code | MNI |
Date Received | 2020-03-14 |
Catalog Number | UNK_SPE |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | K2M, INC. |
Manufacturer Address | 600 HOPE PARKWAY SE LEESBURG VA 20175 US 20175 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-14 |