FDA Adverse Event Malfunction Summary report: N

CD HORIZON SPINAL SYSTEM

MDR report key: 11894897 · Received May 27, 2021

Report

Report Number
1030489-2021-00705
Event Type
Malfunction
Date Received
May 27, 2021
Report Date
May 27, 2021
Manufacturer
WARSAW ORTHOPEDICS
Product Code
KWP
PMA / PMN Number
SEE H10
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

SIMILAR PRODUCT WITH PRODUCT# 8699120 AND 510(K)# - K981676 IS MARKETED IN US. THUS, IT IS REPORTABLE FOR MALFUNCTION, NOT SERIOUS INJURY, ALTHOUGH SURGICAL INTERVENTION DID TAKE PLACE. NEITHER THE DEVICE NOR FILMS OF APPLICABLE IMAGING STUDIES WERE RETURNED TO THE MANUFACTURER FOR EVALUATION. THEREFORE, WE ARE UNABLE TO DETERMINE THE DEFINITIVE CAUSE OF THE REPORTED EVENT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

INFORMATION WAS RECEIVED FROM HEALTHCARE PROVIDER (HCP) VIA A MANUFACTURER REPRESENTATIVE REGARDING A PATIENT, IN SURGERY ON (B)(6) 2018, PSF WAS PERFORMED AT L3-S2AI AND TLIF WAS PERFORMED AT L5 / S1. PRE-OPERATIVE DIAGNOSIS FOR THIS PROCEDURE WAS LUMBAR SPINAL CANAL STENOSIS. REASON FOR REVISION WAS PSEUDOARTHROSIS OF L5/S1, LUMBAR SPINAL CANAL STENOSIS. IT WAS REPORTED THAT ROD BREAKAGE OCCURRED ON BOTH SIDES BETWEEN L5 / S1  PROBABLY DUE TO THE INFLUENCE OF L5 / S1 PSEUDOARTHROSIS. IN THE OPERATION THIS TIME, TLIF WAS PERFORMED AGAIN AT L5 / S1 AND ROD R EPLACEMENT WAS PERFORMED. NO PATIENT SYMPTOMS OR COMPLICATIONS AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
793736 CD HORIZON SPINAL SYSTEM APPLIANCE, FIXATION, SPINAL INTERLAMINAL KWP WARSAW ORTHOPEDICS G8699120 0637417W

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention