FDA Adverse Event Malfunction Summary report: N

CD HORIZON SOLERA SPINAL SYSTEM

MDR report key: 8447592 · Received March 25, 2019

Report

Report Number
1030489-2019-00316
Event Type
Malfunction
Date Received
March 25, 2019
Date of Event
October 15, 2018
Report Date
March 25, 2019
Manufacturer
WARSAW ORTHOPEDICS
Product Code
KWP
PMA / PMN Number
SEE H10
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS PART CONTAINS 4 SET SCREWS OF PART# 6430530. THIS PART IS NOT APPROVED FOR USE IN THE US, HOWEVER, A LIKE DEVICE WITH PART# 6430530, 510K# K143375 AND UPN (B)(4) IS AVAILABLE FOR USE IN THE US. PRODUCT ANALYSIS: MACROSCOPIC AND OPTICAL EXAMINATION REVEALED THREAD CREST/FLANK DAMAGE; THIS DAMAGE APPEARS TO HAVE INITIATED NEAR THE START OF THE THREAD, AND IS EVIDENT AROUND THE DAMAGED PORTION OF THE THREAD. THE ABOVE OBSERVATIONS ARE CONSISTENT WITH MISALIGNMENT OF THE MAS AND SET SCREW THREADS DURING CONSTRUCT ASSEMBLY. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

PRE-OPERATIVE DIAGNOSIS: SPINAL CANAL STENOSIS PROCEDURE: POSTERIOR FUSION AFTER OBLIQUE LUMBAR INTERBODY FUSION (OLIF) IT WAS REPORTED THAT INTRA-OP, WHEN TRYING TO PERFORM FINAL TIGHTENING FROM ONE SIDE OF L3, IT COULD NOT BE THREADED BECAUSE OF IDLE. EVEN THOUGH THE SCREW AND SET SCREW WERE REPLACED, IT WAS THE SAME. WHEN INSERTING THE SET SCREW, A LITTLE SQUEAK SOUND WAS HEARD. COUNTER TORQUE WAS USED. PRODUCT CAME IN CONTACT WITH THE PATIENT. PATIENT COMPLICATIONS WERE REPORTED AS UNKNOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
242475 CD HORIZON SOLERA SPINAL SYSTEM APPLIANCE, FIXATION, SPINAL INTERLAMINAL KWP WARSAW ORTHOPEDICS NA 0651074W

Patients

Seq Age Sex Outcome Treatment
1