ZERO-P IMPLANT 6MM HEIGHT CONVEX-STERILE 04.617.136S

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 2020-02-07 for ZERO-P IMPLANT 6MM HEIGHT CONVEX-STERILE 04.617.136S manufactured by Oberdorf Synthes Produktions Gmbh.

MAUDE Entry Details

Report Number8030965-2020-00970
MDR Report Key9683641
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-07
Date of Report2020-01-18
Date of Event2020-01-18
Date Mfgr Received2020-03-03
Date Added to Maude2020-02-07
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 G1WERK MEZZOVICO (CH)
Manufacturer StreetVIA CAVAZZ 5
Manufacturer CityMEZZOVICO 6805
Manufacturer CountrySZ
Manufacturer Postal Code6805
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameZERO-P IMPLANT 6MM HEIGHT CONVEX-STERILE
Generic NameINTERVERTEBRAL FUSION DEVICE W/INTEGRATED FIXATION,CERVICAL
Product CodeOVE
Date Received2020-02-07
Returned To Mfg2020-03-03
Catalog Number04.617.136S
Lot Number2L02305
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerOBERDORF SYNTHES PRODUKTIONS GMBH
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-07

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