T2 STRATOSPHERE EXPANDABLE CORPECTOMY SYSTEM 436120C

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 2020-03-11 for T2 STRATOSPHERE EXPANDABLE CORPECTOMY SYSTEM 436120C manufactured by Medtronic Sofamor Danek Usa, Inc.

Event Text Entries

[188475189] Product was not returned to the manufacturer for evaluation. Therefore, we are unable to determine the definitive cause of the reported event. Radiographic image review result: three images provided for l2 corpectomy with anterior instrumentation and l1-l3 posterior stabilization. The first ap x-ray shows the interbody cage translated out of the corpecting defect. The second image shows the endcap not in contact with the l1 interior end plate. The third image shows contact with the end plate. It is probable that the cage chipped and lost contact with the endplates along it to translate laterally. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[188475190] It was reported that the patient underwent anterior vertebral body replacement at l2 due to burst fracture. Post-op, t3 backed out after it was inserted. Hence on (b)(6) 2020, during revision surgery, a patient position was taken and it was confirmed by checking the image that the implant has not been in contact with the endplate on the cranial side at all. It was performed after posterior fixation. The reason considered for backing out were the posterior screw loosened, and the anterior side opened. The t3 shrank after the operation. The third image was the image that was taken immediately after the operation. The frontal image right after the operation was not available, but it was considered that the position where the cage was placed had deviated a little from the center of the vertebral body. It was found that it has turned to the state of the first image three or four days after the initial surgery. The second image was taken during the revision surgery. When the implant was placed for the first time, it is unknown at this point that the implant has shrunk or the adjustable end cap was deviated. According to surgeon may be l3 had have compression fracture(it was unknown when compression fracture occurred). The product has been replaced with another implant on (b)(6). There were no other patient complications as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1030489-2020-00299
MDR Report Key9822049
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-11
Date of Report2020-03-11
Date of Event2020-02-14
Date Mfgr Received2020-02-14
Date Added to Maude2020-03-11
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 SOFAMOR DANEK USA, INC
Manufacturer Street4340 SWINEA RD
Manufacturer CityMEMPHIS TN 38118
Manufacturer CountryUS
Manufacturer Postal Code38118
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameT2 STRATOSPHERE EXPANDABLE CORPECTOMY SYSTEM
Generic NameSPINAL VERTEBRAL BODY REPLACEMENT DEVICE
Product CodeMQP
Date Received2020-03-11
Model NumberNA
Catalog Number436120C
Lot NumberCA18J204
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC SOFAMOR DANEK USA, INC
Manufacturer Address4340 SWINEA RD MEMPHIS TN 38118 US 38118


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-11

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