KRAUS K-HELIX PISTON 757-300

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2010-06-01 for KRAUS K-HELIX PISTON 757-300 manufactured by Grace Medical.

Event Text Entries

[22053688] The surgeon had reported that she felt the problem for the displacement was due to the cement. No additional information is expected.
Patient Sequence No: 1, Text Type: N, H10


[22099393] It was reported that the surgeon used ha cement to attach the kraus k-helix piston prosthesis to the incus during surgery. A revision surgery was performed. The prosthesis had come loose and had dropped into the vestibule post-op.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1057421-2010-00001
MDR Report Key1712857
Report Source05
Date Received2010-06-01
Date of Report2010-06-01
Date of Event2010-05-06
Date Mfgr Received2010-05-06
Date Added to Maude2010-06-09
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 ContactBILL GRAHAM, MANAGER
Manufacturer Street8500 WOLF LAKE DR., STE. 110
Manufacturer CityMEMPHIS TN 38133
Manufacturer CountryUS
Manufacturer Postal38133
Manufacturer Phone9013860990
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKRAUS K-HELIX PISTON
Generic NamePARTIAL OSSICULAR REPLACEMENT PROSTHESIS
Product CodeETB
Date Received2010-06-01
Catalog Number757-300
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerGRACE MEDICAL
Manufacturer AddressMEMPHIS TN US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2010-06-01

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