MAUDE Adverse Event Report: GLOBUS MEDICAL, INC. XTEND; XTEND ANTERIOR CERVICAL PLATE, 3-LEVEL, 54MM

Model Number 161.354

Device Problem Insufficient Information (3190)

Patient Problem Insufficient Information (4580)

Event Date 03/22/2019

Event Type  malfunction  

Manufacturer Narrative

This report is being resubmitted for an incident that occurred earlier.The device was not returned for evaluation as it remains in the patient.No determinations can be made as to the cause of the reported issue.

Event Description

It was reported that one screw had backed out of the xtend plate post-operatively.This is the second occurence following a previous revision in (b)(6)2019.

• Brand Name: XTEND
• Type of Device: XTEND ANTERIOR CERVICAL PLATE, 3-LEVEL, 54MM
• Manufacturer (Section D): GLOBUS MEDICAL, INC.; 2560 general armistead avenue; audubon PA 19403
• Manufacturer (Section G): GLOBUS MEDICAL, INC.; 2560 general armistead avenue; audubon PA 19403
• Manufacturer Contact: daniel paul ; 2560 general armistead avenue; audubon, PA 19403 ; 6109301800
• MDR Report Key: 18828778
• MDR Text Key: 336873051
• Report Number: 3004142400-2019-00040
• Device Sequence Number: 1
• Product Code: KWQ
• UDI-Device Identifier: 00849044088168
• UDI-Public: 00849044088168
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K092146
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 03/04/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/04/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: 161.354
• Date Manufacturer Received: 05/08/2019
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Age: 42 YR
• Patient Sex: Male