VERTEBRAL SPACER-TR 10MMX27MM 11MM HEIGHT 889.836S

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 2020-01-03 for VERTEBRAL SPACER-TR 10MMX27MM 11MM HEIGHT 889.836S manufactured by Oberdorf Synthes Produktions Gmbh.

MAUDE Entry Details

Report Number8030965-2020-00036
MDR Report Key9548085
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-01-03
Date of Report2019-12-09
Date of Event2019-01-01
Date Mfgr Received2019-12-09
Date Added to Maude2020-01-03
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 ContactKARA DITTY-BOVARD
Manufacturer StreetEIMATTSTRASSE 3
Manufacturer CityOBERDORF 4436
Manufacturer CountrySZ
Manufacturer Postal4436
Manufacturer Phone6103142063
Manufacturer G1SYNTHES SELZACH
Manufacturer StreetBOHACKERWEG 5
Manufacturer CitySELZACH 2545
Manufacturer CountrySZ
Manufacturer Postal Code2545
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVERTEBRAL SPACER-TR 10MMX27MM 11MM HEIGHT
Generic NameMANDIBLE DISTRACTION DEVICES
Product CodeMQP
Date Received2020-01-03
Catalog Number889.836S
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOBERDORF SYNTHES PRODUKTIONS GMBH
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.