OPTETRAK CONSTRAINED CONDYLAR TIBIAL INSERT 208-23-13

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 2014-01-27 for OPTETRAK CONSTRAINED CONDYLAR TIBIAL INSERT 208-23-13 manufactured by Exactech Inc.

Event Text Entries

[22265125] Revision of equinoxe shoulder components due to infection. Event was discovered through exactech clinical research. The surgeon stated the device may not be directly the cause.
Patient Sequence No: 1, Text Type: D, B5


[22365493] The contribution of the devices to the experience reported could not be determined as the devices were not returned for evaluation. Additionally, the device specific identification information was not provided, precluding a review of the device history record.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1038671-2014-00019
MDR Report Key3641497
Report Source07
Date Received2014-01-27
Date of Report2014-02-10
Date of Event2014-01-08
Date Added to Maude2014-03-28
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 ContactGRAHAM CUTHBERT
Manufacturer Street2320 NW 66TH COURT
Manufacturer CityGAINESVILLE FL 32653
Manufacturer CountryUS
Manufacturer Postal32653
Manufacturer Phone8003922832
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOPTETRAK CONSTRAINED CONDYLAR TIBIAL INSERT
Generic NameTIBIAL INSERT
Product CodeHSH
Date Received2014-01-27
Catalog Number208-23-13
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEXACTECH INC
Manufacturer Address2320 N.W. 66TH CT. GAINESVILLE FL 32653 US 32653


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2014-01-27

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