FDA Adverse Event Malfunction Summary report: N

KYPHON XPEDE BONE CEMENT

MDR report key: 23507639 · Received November 10, 2025

Report

Report Number
6000033-2025-00134
Event Type
Malfunction
Date Received
November 10, 2025
Date of Event
October 15, 2025
Report Date
November 10, 2025
Manufacturer
CARDIAC SURGERY MFG KERKRADE
Product Code
NDN
UDI-DI
00763000269807
PMA / PMN Number
SEE H11
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

G2: THE COUNTRY OF THE EVENT IS GERMANY. G4. PLEASE NOTE THAT THIS DEVICE (CX01B-C) IS NOT MARKETED IN THE UNITED STATES; HOWEVER, IT IS SAME TO THE UNITED STATES MARKETED DEVICE WITH CATALOG # CX01B, 510K# K102397 AND UDI # (B)(4). MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.

Description of Event or Problem · 0

INFORMATION WAS RECEIVED FROM HEALTHCARE PROVIDER (HCP) VIA A MANUFACTURER REPRESENTATIVE REGARDING A DEVICE USED FOR KYPHOPLASTY PROCEDURE. IT WAS REPORTED THAT THE CEMENT SET TOO QUICKLY AND COULD NO LONGER BE USED. THERE WAS NO PATIENT INVOLVED AS THE EVENT OCCURRED DURING INITIAL SETUP. THE PROCEDURE WAS COMPLETED SUCCESSFULLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1807946 KYPHON XPEDE BONE CEMENT CEMENT, BONE, VERTEBROPLASTY NDN CARDIAC SURGERY MFG KERKRADE CX01B-C 232079450 00763000269807

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown