TELEPORT 9044-00

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2011-02-28 for TELEPORT 9044-00 manufactured by Interventional Spine, Inc..

Event Text Entries

[16037980] The surgeon released the final stage on the disposal teleport; unable to budge the "pull 2" button. Surgeon used a mallet and tapped it. The button finally worked and the case was completed.
Patient Sequence No: 1, Text Type: D, B5


[16093595] Root cause: loose metallic debris: loose metallic debris was present because, the component was not properly deburred. Initially, it was determined, the event was not reportable. On a subsequent re-review, it was determined that this event should have been reported.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2032499-2011-00025
MDR Report Key2045711
Report Source99
Date Received2011-02-28
Date of Report2009-06-03
Date Mfgr Received2009-06-03
Device Manufacturer Date2009-03-01
Date Added to Maude2012-02-10
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 FDA0
Event Location0
Manufacturer Street13700 ALTON PKWY, SUITE 160
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9494720006
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTELEPORT
Product CodeMRW
Date Received2011-02-28
Model Number9044-00
Catalog Number9044-00
Lot Number020609-B
Device Expiration Date2011-01-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerINTERVENTIONAL SPINE, INC.
Manufacturer AddressIRVINE CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2011-02-28

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