MAUDE Adverse Event Report: ULRICH MEDICAL USA SOLIDITY; CENTER PIECE, LIGHT BLUE, DIA 13MM, HEIGHT 13-17.5MM TWO FIXED ANGULATION PLATES

Model Number	UU041-01-1317
Medical Device Problem Code	Collapse (1099)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/22/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported during a post operative follow up the vbr cage had collapsed.There was no effect on the patient and there was no need for a revision surgery.

• Brand Name: SOLIDITY
• Common Device Name: CENTER PIECE, LIGHT BLUE, DIA 13MM, HEIGHT 13-17.5MM TWO FIXED ANGULATION PLATES
• Manufacturer (Section D): ULRICH MEDICAL USA; 3700 east plano parkway; suite 200; plano TX 75074
• Manufacturer (Section G): ULRICH GMBH & CO. KG; buchbrunnenweg 12; ulm, baden-wurttemberg 89081 ; GM 89081
• Manufacturer Contact: louis milos ; 3700 east plano parkway; suite 200; plano, TX 75074 ; 4692380832
• MDR Report Key: 19392013
• Report Number: 3005823819-2024-00006
• Device Sequence Number: 7799435
• Product Code: MQP
• UDI-Device Identifier: 00814386022279
• UDI-Public: 00814386022279
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K181921
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/16/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: UU041-01-1317
• Device Catalogue Number: UU041-01-1317
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/18/2024
• Initial Report FDA Received Date: 05/24/2024
• 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
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization
• Patient Age: 51 YR
• Patient Sex: Prefer Not To Disclose