ATLAS? CABLE SYSTEM 826-211

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2013-06-24 for ATLAS? CABLE SYSTEM 826-211 manufactured by Warsaw Orthopedic, Inc..

Event Text Entries

[3517932] It was reported that a patient underwent an unknown procedure. At an unknown time post-op it was noted that the leader on the cable broke. No further details are known at this time.
Patient Sequence No: 1, Text Type: D, B5


[10750580] (b)(6). (b)(4). 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.
Patient Sequence No: 1, Text Type: N, H10


[20903381] Analysis of the returned device confirms that the leader fragmented from the cable. Optical inspection did not identify witness marks or plastic deformation along the length of the cable. The location of the fracture is located at the welded joint. Weld diameter found to be conforming to print specification. The morphology of the fracture is consistent with tensile overload. The above observations are consistent with overload.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1030489-2013-02472
MDR Report Key3185984
Report Source05,07
Date Received2013-06-24
Date of Report2013-07-15
Date of Event2013-06-14
Date Mfgr Received2013-07-15
Date Added to Maude2013-08-26
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 ContactHUZEFA MAMOOLA
Manufacturer Street1800 PYRAMID PLACE
Manufacturer CityMEMPHIS TN 38132
Manufacturer CountryUS
Manufacturer Postal38132
Manufacturer Phone9013963133
Manufacturer G1MEDTRONIC SOFAMOR DANEK
Manufacturer Street1800 PYRAMID PLACE
Manufacturer CityMEMPHIS TN 38132
Manufacturer CountryUS
Manufacturer Postal Code38132
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameATLAS? CABLE SYSTEM
Generic NameCABLE
Product CodeISN
Date Received2013-06-24
Returned To Mfg2013-06-26
Catalog Number826-211
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerWARSAW ORTHOPEDIC, INC.
Manufacturer Address2500 SILVEUS CROSSING WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
10 2013-06-24

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.