FDA Adverse Event Injury Summary report: N

MID-C 125

MDR report key: 10818240 · Received November 10, 2020

Report

Report Number
3013461531-2020-00009
Event Type
Injury
Date Received
November 10, 2020
Date of Event
August 14, 2020
Report Date
September 29, 2020
Manufacturer
APIFIX LTD
Product Code
QGP
UDI-DI
07290014993068
PMA / PMN Number
H170001
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

A REVIEW OF THE DHR DEMONSTRATED THAT THE MID-C SYSTEM WAS MANUFACTURED, TESTED, AND RELEASED ACCORDING TO APIFIX SPECIFICATIONS. THE X-RAY DEMONSTRATES THAT THE SYSTEM REACHED ITS MAXIMAL ELONGATION, WHICH IS THE WEAKEST POINT OF THE ROD. THUS, THE TRANSVERSE PROCESS BELOW THE IMPLANT MAY GENERATE A FORCE ACTING ON THE SYSTEM THAT CAN CAUSE THE ROD BREAKAGE. TO PROTECT AGAINST SUCH FORCE IT IS NECESSARY TO USE THE TRIAL TOOL ACCORDING TO THE DETAILED STEPS AS DESCRIBED IN THE SURGICAL TECHNIQUE GUIDE. THE SURGERY WAS PERFORMED IN A MINIMAL INVASIVE APPROACH (MIS), WHICH MAKES IT VERY CHALLENGING TO VERIFY THAT THE SURFACE BELOW THE IMPLANT IS SUFFICIENTLY CLEAN FROM ANY SOFT OR HARD TISSUE BEFORE PLACING THE IMPLANT. FOR THIS REASON, THE USE OF MIS TECHNIQUE IS NOT RECOMMENDED BY THE COMPANY AND THE SURGICAL TECHNIQUE INSTRUCTS TO PERFORM THE SURGERY WITH AN OPEN MIDLINE INCISION. AT THE TIME OF THIS REPORT (AUG 2020), THE COMPANY'S INCIDENT RATE DUE TO IMPLANT BREAKAGE AT MAXIMAL ELONGATION IS 0.98% AND THE OVERALL FOR THIS CATEGORY IS 6.50%, WHICH IS WELL WITHIN THE RATE REPORTED IN THE LITERATURE FOR THIS CATEGORY ( 0.2%-15.5%) ( CER DMS-727 REV R). THE RISK OF THE BROKEN ROD HAS BEEN ASSESSED AND FOUND TO BE ACCEPTABLE (DMS#777 REV Q1 HAZARD ID 1.8) BESIDES, THE COMPANY HAS IMPLEMENTED CORRECTIVE ACTION RESULTING IN AN UPDATED DESIGN OF THE MID-C 125 WITH ELONGATION OF 50 MM, HAVING LONGER OVERLAP BETWEEN POLE AND BASE WHICH MITIGATE AGAINST CASES OF MAXIMAL ELONGATION.

Description of Event or Problem · 1

THE X-RAY ON (B)(6) 2020 DEMONSTRATED ON OMPLANT BREAKAGE. THE SURGEON IS RELUCTANT TO DO ANYTHING AT THIS TIME BECAUSE HER CORRECTION IS STILL AT <10 DEGREES AND OTHERWISE ASYMPTOMATIC.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1285215 MID-C 125 POSTERIOR RATCHETING ROD SYSTEM, QGP APIFIX LTD MID-C 125 AF 09-01-17 07290014993068

Patients

Seq Age Sex Outcome Treatment
1 16 YR