MAUDE Adverse Event Report: ASTURA MEDICAL ASTURA; LLIF SPACER

Model Number	GB225510B
Medical Device Problem Code	Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	Implant Pain (4561)
Date of Event	06/11/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Items from the same lot were tested and work as they should.Original receiving inspection reports show implants to be in specification.Implant was not broken and was still intact in the patient.
Event or Problem Description
Implant backed out requiring a revision surgery.

• Brand Name: ASTURA
• Common Device Name: LLIF SPACER
• Manufacturer (Section D): ASTURA MEDICAL; 4949 w. royal lane; irving TX 75063
• Manufacturer (Section G): ASTURA MEDICAL; 4949 w. royal ln.; irving TX 75063
• Manufacturer Contact: parker kelch ; 4949 w. royal ln.; irving, TX 75063 ; 4695015530
• MDR Report Key: 22893602
• Report Number: 3015941638-2025-00006
• Device Sequence Number: 5828268
• Product Code: OVD
• UDI-Device Identifier: 00840085225208
• UDI-Public: 00840085225208
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K192006
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 08/25/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: GB225510B
• Device Catalogue Number: GB225510B
• Device Lot Number: 417115B
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 07/29/2025
• Initial Report FDA Received Date: 08/26/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: N/A
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 60 YR
• Patient Sex: Female
• Patient Weight: 91 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White