MAUDE Adverse Event Report: ENDOLOGIX SANTA ROSA OVATION IX; EXTENDER

Model Number TV-EX222245-J

Device Problem Lack of Effect (4065)

Event Date 03/20/2024

Event Type  Injury  

Event Description

The patient was implanted with the alto stent graft system to treat an abdominal aortic aneurysm (aaa).Approximately two and half (2.5) years post initial procedure, during routine follow-up, a type 1b endoleak was suspected but confirmed to be a type 3a endoleak.The physician elected to implant non-endologix coils and an ovation ix iliac limb to resolve this event.The patient was reported as stable post secondary procedure.

Manufacturer Narrative

The device involved in this event will not be returned for evaluation as it remains implanted in the patient.Patient medical records and imaging studies will be requested for further evaluation by the clinical specialist.If additional information pertinent to the incident is obtained, a follow-up report will be submitted.H3 other text : device remans implanted.

Manufacturer Narrative

The reported adverse event/incident was investigated in alignment with endologix operating procedures and work instructions.Where possible, it is endologix practice to make at least three good faith efforts to retrieve a reported adverse event/incident related device as well as medical records and medical imaging.An evaluation of the manufacturing record was completed.A review of the part number/lot number combination needed for device identification shows the device to have been properly manufactured and released in accordance with the device master record.The review confirms there were no manufacturing or processing non-conformities identified that would contribute to the reported adverse event/incident.An evaluation of the device could not be completed.The device was not returned to endologix for evaluation because it remains implanted.A clinical evaluation of the adverse event/incident could not be completed.No medical records nor medical imaging relevant to the reported adverse event/incident was received by endologix.The user facility was unable to provide this information.No additional investigation of this reported adverse event/incident is planned.However, should additional information relevant to the investigation outcome become available, a follow-up report will be submitted.Endologix will continue to monitor this and similar adverse events/incidents.Corrections: (b)(4).

• Brand Name: OVATION IX
• Type of Device: EXTENDER
• Manufacturer (Section D): ENDOLOGIX SANTA ROSA; 3910 brickway blvd; santa rosa CA 95403
• Manufacturer (Section G): ENDOLOGIX SANTA ROSA; 3910 brickway blvd; ,; santa rosa CA 95403
• Manufacturer Contact: gary kirchgater ; 3910 brickway blvd; ,; santa rosa, CA 95403 ; 8009832284
• MDR Report Key: 19058225
• MDR Text Key: 339557476
• Report Number: 3008011247-2024-00038
• Device Sequence Number: 1
• Product Code: MIH
• UDI-Device Identifier: M701TVEX222245J1
• UDI-Public: +M701TVEX222245J1/$$3230717FS07172009
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: P120006
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Health Professional,Company Representative
• Reporter Occupation: Physician
• Remedial Action: Other
• Type of Report: Initial,Followup
• Report Date: 03/20/2024

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
• Device Operator: Health Professional
• Device Expiration Date: 07/17/2023
• Device Model Number: TV-EX222245-J
• Device Lot Number: FS071720-09
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 03/20/2024
• Initial Date FDA Received: 04/08/2024
• Supplement Dates Manufacturer Received: Not provided
• Supplement Dates FDA Received: 05/28/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 08/05/2020
• 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
• Treatment: ALTO MAIN BODY, LOT # FS012921-25; OVATION IX ILIAC LIMB, LOT # FS011121-23; OVATION IX ILIAC LIMB, LOT # FS050421-39; OVATION IX ILIAC LIMB, LOT # FS072220-21; OVATION PRIME FILL POLYMER, LOT # FF010521-01
• Patient Outcome(s): Required Intervention
• Patient Age: 94 YR
• Patient Sex: Male