FDA Adverse Event Injury Summary report: N

PIONEER SURGICAL TECHNOLOGY STREAMLINE TL

MDR report key: 18859262 · Received March 7, 2024

Report

Report Number
1833824-2024-00035
Event Type
Injury
Date Received
March 7, 2024
Report Date
March 7, 2024
Manufacturer
PIONEER SURGICAL TECHNOLOGY
Product Code
NKB
UDI-DI
00846468005573
PMA / PMN Number
K140696
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

"DEVICE WAS NOT RETURNED TO RESOLVE SURGICAL FOR INSPECTION. MULTIPLE ATTEMPTS WERE MADE TO GATHER DATA FROM THE REP. NO ADDITIONAL INFORMATION OR CONFIRMATION HAS BEEN GIVEN THAT THIS IS A PIONEER SURGICAL TECHNOLOGIES MANUFACTURED PART. THE FOLLOWING SECTIONS OF THIS REPORT HAVE BEEN LEFT BLANK DUE TO THE INFORMATION BEING UNAVAILABLE OR NON-APPLICABLE: A1-A6, B3, B6-B7, D6A, G5, G7-G8, H2, H7, H9-H10.

Description of Event or Problem · 0

OUR OEM DISTRIBUTION REP "XTANT MEDICAL HAS RECEIVED A PRODUCT COMPLAINT FROM THE STREAMLINE TL SPINAL FIXATION SYSTEM, IN WHICH IT WAS REPORTED THAT TWO PEDICLE SCREW IMPLANTS (01-PA-55-45, LOTS 378753 AND 388226) WERE IDENTIFIED AS BROKEN, WHICH REQUIRED A REVISION PROCEDURE. XTANT MEDICAL HAS INITIATED COMPLAINT 24-024 ON THE ISSUE. ATTACHED IS THE IMAGING PROVIDED BY THE COMPLAINT SOURCE. BELOW IS RELEVANT INFORMATION PROVIDED BY THE COMPLAINT SOURCE, PLEASE LET ME KNOW IF YOU HAVE ANY QUESTIONS OR CONCERNS, APPRECIATE THE ASSISTANCE. INDEX PROCEDURE PERFORMED (B)(6) 2022, REVISION PROCEDURE PERFORMED (B)(6) 2024".

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2163459 PIONEER SURGICAL TECHNOLOGY STREAMLINE TL THORACOLUMBOSACRAL PEDICLE SCREW SYSTEM NKB PIONEER SURGICAL TECHNOLOGY 01-PA-55-45 378753 00846468005573

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Other