MAUDE Adverse Event Report: SYNTHES GMBH XRL MED ENDPLATE 21MM X 24MM/5 DEG-ST; SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

Model Number 08.807.234S

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Non-union Bone Fracture (2369)

Event Type  Injury  

Manufacturer Narrative

Without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

Event Description

This report is being filed after the review of the following journal article: deml mc, et al.(2020), anterior column reconstruction of the thoracolumbar spine with a new modular peek vertebral body replacement device: retrospective clinical and radiologic cohort analysis of 48 cases with 1.7-years follow-up, european spine journal, volume 29, pages 3194¿3202 (switzerland).The purpose of this retrospective study is to evaluate whether a new peek vertebral body replacement can maintain the sagittal alignment as an anterior column reconstruction device in thoracic and lumbar spinal defects due to trauma or tumor.Between august 2013 to may 2017, 48 patients who underwent a corpectomy between t5 and l5 due to trauma or tumor and were stabilized with the new peek vertebral body replacement were included in the study.There were 30 males and 18 females with a mean age of 43.0+/-15.3 years (range, 18-72).There were 14 procedures performed in a single- and 34 in a two-stage-procedure.For anterior column reconstruction, the modular, expandable unknown synthes expandable xrl peek vertebral body replacement device was used.Patients were followed up at 2, 6, 12 and 24 months postoperatively.Each patient received previously or during the same procedure an open or percutaneous posterior instrumentation with or without decompression.Complications were reported as follows: 2 patients had a ¿probably not fused status' due to cage malpositioning.1 patient had an epidural hematoma with neurologic deficit which needed immediate revision surgery.Neurologic symptoms recovered to normal during further follow-up.A (b)(6) female patient had a posterior implant failure with breakage of a pedicle screw, secondary cranial and caudal subsidence of the cage and incomplete osseous consolidation.The patient refused revision surgery.This report is for xrl med endplate 21mm x 24mm/10 deg-st.This is report 5 of 6 for (b)(4).

• Brand Name: XRL MED ENDPLATE 21MM X 24MM/5 DEG-ST
• Type of Device: SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): MONUMENT; 1101 synthes avenue; monument CO 80132
• Manufacturer Contact: kara ditty-bovard ; 1302 wrights lane east; west chester, PA 19380 ; 6103142063
• MDR Report Key: 12268374
• MDR Text Key: 264793566
• Report Number: 8030965-2021-06368
• Device Sequence Number: 1
• Product Code: MQP
• UDI-Device Identifier: 10705034755427
• UDI-Public: (01)10705034755427
• Combination Product (y/n): N
• Reporter Country Code: SZ
• PMA/PMN Number: K103320
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 07/06/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/03/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: 08.807.234S
• Device Catalogue Number: 08.807.234S
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 07/06/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention