MAUDE Adverse Event Report: MITG - TIJUANA KYPHON® EXPRESS¿ II INFLATABLE BONE TAMP; ARTHROSCOPE

Model Number	KE152
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/25/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
Event or Problem Description
(b)(4) (rep, hcp, for): information was received from healthcare provider (hcp) via a manufacturer representative regarding an event which occurred during a l1 transcutaneous vertebroplasty procedure in a patient diagnosed with compression fracture due to primary osteoporosis.Patient medical history: hypertension, hyperlipidemia, appendicitis, cataract, cerebral infarction, bronchial asthma.It was reported that when the balloon was inserted and inflated, it ruptured at 310psi.There was no patient symptom reported.There were no further complications reported regarding the event.

• Brand Name: KYPHON® EXPRESS¿ II INFLATABLE BONE TAMP
• Common Device Name: ARTHROSCOPE
• Manufacturer (Section D): MITG - TIJUANA; blvd. insurgentes parcela #37; tijuana, bc 22570 ; MX 22570
• Manufacturer (Section G): MITG - TIJUANA; blvd. insurgentes parcela #37; tijuana, bc 22570 ; MX 22570
• Manufacturer Contact: justin ellis ; 1800 pyramid place; memphis, TN 38132 ; 7635265677
• MDR Report Key: 22976503
• Report Number: 2936999-2025-00441
• Device Sequence Number: 9708965
• Product Code: HRX
• UDI-Device Identifier: 00763000312039
• UDI-Public: 00763000312039
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K123771
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 09/05/2025

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: KE152
• Device Catalogue Number: KE152
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/25/2025
• Initial Report FDA Received Date: 09/05/2025
• 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
• Patient Sex: Unknown