TGS UKA KNEE SYSTEM
Report
- Report Number
- 3004594167-2013-00007
- Event Type
- Injury
- Date Received
- September 10, 2013
- Date of Event
- August 14, 2013
- Report Date
- September 10, 2013
- Manufacturer
- ALEXANDRIA RESEARCH TECHNOLOGIES, INC.
- Product Code
- HSX
- PMA / PMN Number
- K090024
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
EVENT IS BEING REPORTED WITH INFORMATION THAT IS AVAILABLE TO COMPLY WITH THE 30 DAY REPORTING REQUIREMENT. ON THREE OCCASIONS ADDITIONAL INFORMATION HAS BEEN REQUESTED TO CONFIRM THE REVISION SURGERY AND TO GATHER ADDITIONAL DATA, HOWEVER, A RESPONSE IS YET TO BE PROVIDED. IF ADDITIONAL INFORMATION IS RECEIVED REGARDING THE REVISION PROCEDURE, THE COMPLAINT WILL BE REASSESSED AND A FOLLOW UP REPORT WILL BE SUBMITTED. REVIEW OF DEVICE HISTORY RECORDS SHOW THAT THE LOW WAS RELEASED WITH NO ISSUES AND PRODUCT WAS MANUFACTURED TO SPEC. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. PMA: 510 (K) #K090024, COVERS INITIAL RELEASE OF TGS UKA SYSTEM INCLUDING ALL INSTRUMENTATION AND FEMORAL COMPONENT, PMA 510 (K) #K101206, COVERS THE TIBIAL BASEPLATE COMPONENT AND TIBIAL INSERT COMPONENT. ADD'L INFO: TIBIAL BASEPLATE: LOT: 1103009-A, CATALOG: 100294, MFG. DATE: 10/2012, EXP. DATE: 10/2015. TIBIAL INSERT: LOT: 1103026-A, CATALOG #: 100313, MFG. DATE: 06/2011, EXP. DATE: 06/2014.
ON (B)(6) 2013, IT WAS REPORTED THAT A PATIENT WITH THE INITIALS (B)(6) WAS SCHEDULED FOR REVISION SURGERY TO REPLACE A TGS UKA KNEE IMPLANT AND THAT THE REVISION WAS SCHEDULED FOR (B)(6) /2013.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 453710 | TGS UKA KNEE SYSTEM | UNICOMPARTMENTAL KNEE ARTHROPLASTY (UKA) | HSX | ALEXANDRIA RESEARCH TECHNOLOGIES, INC. | 1111001-A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 66 YR | Hospitalization| R |