KYPHON XPANDER INFLATABLE BONE TAMP K09A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-12-07 for KYPHON XPANDER INFLATABLE BONE TAMP K09A manufactured by Medtronic Mexico (tijuana).

Event Text Entries

[129784257] Neither the device nor films of applicable imaging studies were returned to the manufacturer for evaluation. Therefore, we are unable to determine the definitive cause of the reported event. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[129784258] It was reported that the patient was pre-operatively diagnosed with primary osteoporosis (compression fracture) and underwent unspecified procedure. During the surgery, the balloon was inflated, and it was broken when approaching to the cortical bone of vertebral body. Since it was inflated to the targeted end point, the balloon was deflated, the contrast medium was removed from the patient body, the cement was injected and the procedure was completed successfully with the original product. The product came in contact with the patient. Patient complications were reported as unknown.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9612164-2018-03519
MDR Report Key8144580
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-12-07
Date of Report2019-02-11
Date of Event2018-11-09
Date Mfgr Received2019-01-23
Date Added to Maude2018-12-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactSTACIE ZIEMBA
Manufacturer Street1800 PYRAMID PLACE
Manufacturer CityMEMPHIS TN 38132
Manufacturer CountryUS
Manufacturer Postal38132
Manufacturer Phone9013963133
Manufacturer G1MEDTRONIC MEXICO (TIJUANA)
Manufacturer StreetAVENIDA PASEO CUCAPAH # 10510 PARQUE INDUSTRIAL EI LAGO
Manufacturer CityTIJUANA,BC 22570
Manufacturer CountryMX
Manufacturer Postal Code22570
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKYPHON XPANDER INFLATABLE BONE TAMP
Generic NameTAMP
Product CodeHXG
Date Received2018-12-07
Returned To Mfg2019-01-22
Model NumberNA
Catalog NumberK09A
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC MEXICO (TIJUANA)
Manufacturer AddressAVENIDA PASEO CUCAPAH # 10510 PARQUE INDUSTRIAL EI LAGO TIJUANA,BC 22570 MX 22570


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-07

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