ITOTAL PS TPS-111-1111-020101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-09-14 for ITOTAL PS TPS-111-1111-020101 manufactured by Conformis, Inc..

Event Text Entries

[26169094] A disposable cutting guide broke during surgery. The surgery was completed successfully. Review of the device history record indicates that the device was manufactured to specification.
Patient Sequence No: 1, Text Type: N, H10


[26169095] A disposable cutting guide broke during the case. The surgery was completed successfully.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011705391-2015-00171
MDR Report Key5073725
Date Received2015-09-14
Date of Report2015-09-14
Date of Event2015-08-17
Date Mfgr Received2015-08-18
Device Manufacturer Date2015-08-10
Date Added to Maude2015-09-14
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 ContactKARINA SNOW
Manufacturer Street28 CROSBY DRIVE
Manufacturer CityBEDFORD MA 01730
Manufacturer CountryUS
Manufacturer Postal01730
Manufacturer Phone7813459195
Manufacturer G1CONFORMIS, INC.
Manufacturer Street600 RESEARCH DRIVE
Manufacturer CityWILMINGTON MA 01887
Manufacturer CountryUS
Manufacturer Postal Code01887
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameITOTAL PS
Generic NameTOTAL KNEE REPLACEMENT SYSTEM
Product CodeOOG
Date Received2015-09-14
Catalog NumberTPS-111-1111-020101
Device Expiration Date2016-01-31
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONFORMIS, INC.
Manufacturer Address28 CROSBY DRIVE BEDFORD MA 01730 US 01730


Patients

Patient NumberTreatmentOutcomeDate
10 2015-09-14

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