MAUDE Adverse Event Report: ASTURA MEDICAL ASTURA MEDICAL; METALLIC SPINAL INTERBODY FUSION CAGE

Model Number	BH092409D
Medical Device Problem Code	Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	Implant Pain (4561)
Date of Event	07/31/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Item was returned from hospital and tested and worked as it should.Original receiving inspection reports show implant to be in specification.
Event or Problem Description
Expandable spacer began to migrate out of the disc space, requiring revision surgery.

• Brand Name: ASTURA MEDICAL
• Common Device Name: METALLIC SPINAL INTERBODY FUSION CAGE
• Manufacturer (Section D): ASTURA MEDICAL; 4949 w. royal ln.; 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: 23084769
• Report Number: 3015941638-2025-00008
• Device Sequence Number: 18770957
• Product Code: MAX
• UDI-Device Identifier: 00841379180876
• UDI-Public: 00841379180876
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K182877
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted 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): 09/02/2025

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: BH092409D
• Device Catalogue Number: BH092409D
• Device Lot Number: 793505I
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/05/2025
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 09/05/2025
• Initial Report FDA Received Date: 09/18/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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: 71 YR
• Patient Sex: Male
• Patient Weight: 91 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White