SMART STAPES PISTON 70145928

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2005-08-26 for SMART STAPES PISTON 70145928 manufactured by Gyrus Ent.

Event Text Entries

[411325] It was reported that a patient required a revision surgery post-op a partial ossicular replacement procedure due to a loss of hearing. The implant was explanted and replaced. The surgeon states that the implant was found out of the oval window but still on the incus.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1037007-2005-00006
MDR Report Key631779
Report Source07
Date Received2005-08-26
Date of Report2005-08-26
Date of Event2005-03-18
Date Mfgr Received2005-08-10
Date Added to Maude2005-08-31
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 ContactMR. DOLAN MILLS
Manufacturer Street2925 APPLING RD
Manufacturer CityBARTLETT TN 38133
Manufacturer CountryUS
Manufacturer Postal38133
Manufacturer Phone*
Manufacturer G1GYRUS ENT
Manufacturer Street2925 APPLING ROAD
Manufacturer CityBARTLETT TN 38133
Manufacturer CountryUS
Manufacturer Postal Code38133
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSMART STAPES PISTON
Generic NamePARTIAL OSSICULAR REPLACEMENT PROSTHESIS
Product CodeETB
Date Received2005-08-26
Model NumberNA
Catalog Number70145928
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age06 MO
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key621362
ManufacturerGYRUS ENT
Manufacturer Address* BARTLETT TN 38133 US
Baseline Brand NameSMART
Baseline Generic NamePISTON
Baseline Model NoNA
Baseline Catalog No70145928
Baseline IDNA
Baseline Device FamilySMART STAPES PISTON PROSTHESIS
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK003214
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2005-08-26

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