IUNI G2 M5722INT0600210

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2015-05-08 for IUNI G2 M5722INT0600210 manufactured by Conformis.

Event Text Entries

[5795145] Patient developed an infection. Revision surgery occurred to exchange the poly insert.
Patient Sequence No: 1, Text Type: D, B5


[13429333] Patient developed an infection. Revision surgery occurred to exchange the poly insert. Review of the device history record indicates that the device was manufactured to specification. All sterilization requirements were met.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004153240-2015-00077
MDR Report Key4763213
Report Source01,05
Date Received2015-05-08
Date of Report2015-04-17
Date of Event2015-04-01
Date Mfgr Received2015-04-17
Device Manufacturer Date2015-03-01
Date Added to Maude2015-05-12
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 DRIVE
Manufacturer CityBEDFORD MA 01730
Manufacturer CountryUS
Manufacturer Postal01730
Manufacturer Phone7813459195
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIUNI G2
Generic NameUNICONDYLAR KNEE REPLACEMENT SYSTEM
Product CodeOOG
Date Received2015-05-08
Catalog NumberM5722INT0600210
Device Expiration Date2015-08-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONFORMIS
Manufacturer Address28 CROSBY DRIVE BEDFORD MA 01730 US 01730


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2015-05-08

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