ARTELON CMC SPACER

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 2013-05-06 for ARTELON CMC SPACER manufactured by Artimplant Ab.

Event Text Entries

[18851425] Explantation of artelon stt spacer due to increasing pain at activity. The patient had been pain free and functional until approx 18 months after implant surgery. X-rays revealed recurrent osteophytes. (same patient as 3004878714-2013-00013). (b)(4).
Patient Sequence No: 1, Text Type: D, B5


[19211928] Explant sent for histological analysis. No result yet.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004878714-2013-00014
MDR Report Key3161564
Report Source07
Date Received2013-05-06
Date of Report2013-05-28
Date of Event2013-05-07
Date Mfgr Received2013-05-07
Date Added to Maude2013-06-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer StreetHULDA MELLGRENS GATA 5
Manufacturer CityV. FROLUNDA SE-421 32
Manufacturer CountrySW
Manufacturer PostalSE-421 32
Manufacturer Phone17465600
Manufacturer G1ARTIMPLANT AB
Manufacturer StreetHULDA MELLGRENS GATA 5
Manufacturer CityV. FROLUNDA
Manufacturer CountrySW
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARTELON CMC SPACER
Generic NameSPACER
Product CodeKYI
Date Received2013-05-06
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerARTIMPLANT AB
Manufacturer AddressHULDA MELLGRENS GATA 5 V. FROLUNDA SW


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2013-05-06

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