KALIX FLAT FOOT IMPLANT EXTERNAL DIAM. 10MM * 140010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,08 report with the FDA on 2005-04-20 for KALIX FLAT FOOT IMPLANT EXTERNAL DIAM. 10MM * 140010 manufactured by Newdeal S.a..

Event Text Entries

[401628] Pt originally had the device implanted in 2003. It was alleged that the device broke. A revision operation was performed due to the breakage.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615741-2005-00004
MDR Report Key593662
Report Source06,08
Date Received2005-04-20
Date of Report2005-04-20
Date of Event2004-10-07
Date Mfgr Received2005-03-23
Date Added to Maude2005-04-22
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 Location0
Manufacturer ContactYANPING WANG
Manufacturer Street311 C ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362322
Manufacturer G1NEWDEAL S.A.
Manufacturer Street10 PLACE D'HELVETIE
Manufacturer CityLYON 69006
Manufacturer CountryFR
Manufacturer Postal Code69006
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKALIX FLAT FOOT IMPLANT EXTERNAL DIAM. 10MM
Generic NameKALIX IMPLANT SYSTEM
Product CodeHWL
Date Received2005-04-20
Model Number*
Catalog Number140010
Lot NumberB085
ID Number*
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Implant FlagY
Date Removed*
Device Sequence No1
Device Event Key583502
ManufacturerNEWDEAL S.A.
Manufacturer Address* LYON FR
Baseline Brand NameKALIX FLAT FOOT IMPLANT EXTERNAL DIAM. 10MM
Baseline Generic NameKALIX IMPLANT SYSTEM
Baseline Model No*
Baseline Catalog No140010
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
10 2005-04-20

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