ITOTAL UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 03,05 report with the FDA on 2014-10-01 for ITOTAL UNK manufactured by Conformis.

Event Text Entries

[5094246] Data presented by dr. (b)(6) in a conference presentation indicated that 6 itotal patients required manipulation under anesthesia to improve post-operative range of motion. One manipulation was unsuccessful and the patient was scheduled for revision for arthrofibrosis.
Patient Sequence No: 1, Text Type: D, B5


[12366606] Serial number and device model information was not available. Investigation specific to the affected patients and devices could not be conducted.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004153240-2014-00129
MDR Report Key4185991
Report Source03,05
Date Received2014-10-01
Date of Report2014-09-03
Date Mfgr Received2014-09-03
Date Added to Maude2014-10-21
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 ContactKARINA SNOW
Manufacturer Street28 CROSBY DR.
Manufacturer CityBEDFORD MA 01730
Manufacturer CountryUS
Manufacturer Postal01730
Manufacturer Phone7813459195
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameITOTAL
Generic NameTOTAL KNEE REPLACEMENT SYSTEM
Product CodeHSH
Date Received2014-10-01
Catalog NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONFORMIS
Manufacturer AddressCROSBY DR. BEDFORD MA 01730 US 01730


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2014-10-01

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