TI MATRIXNEURO SCREW SELF-DRILLING 4MM 04.503.104.01S

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-06-14 for TI MATRIXNEURO SCREW SELF-DRILLING 4MM 04.503.104.01S manufactured by Oberdorf Synthes Produktions Gmbh.

MAUDE Entry Details

Report Number8030965-2019-65336
MDR Report Key8700978
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-06-14
Date of Report2019-05-17
Date of Event2019-05-16
Date Mfgr Received2019-06-17
Device Manufacturer Date2018-12-13
Date Added to Maude2019-06-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKARA DITTY-BOVARD
Manufacturer StreetEIMATTSTRASSE 3
Manufacturer CityOBERDORF 4436
Manufacturer CountrySZ
Manufacturer Postal4436
Manufacturer Phone6103142063
Manufacturer G1WERK BETTLACH (CH)
Manufacturer StreetMURACHERSTRASSE 3
Manufacturer CityBETTLACH 2544
Manufacturer CountrySZ
Manufacturer Postal Code2544
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTI MATRIXNEURO SCREW SELF-DRILLING 4MM
Generic NamePLATE,CRANIOPLASTY,PREFORMED, ALTERABLE
Product CodeGWO
Date Received2019-06-14
Returned To Mfg2019-06-03
Catalog Number04.503.104.01S
Lot Number2L72056
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerOBERDORF SYNTHES PRODUKTIONS GMBH
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-14

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