INVICTUS SPINAL FIXATION SYSTEM 17001-01 1700-01

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-12-26 for INVICTUS SPINAL FIXATION SYSTEM 17001-01 1700-01 manufactured by Alphatec Spine Inc.

MAUDE Entry Details

Report Number2027467-2019-00061
MDR Report Key9519501
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-12-26
Date of Report2019-12-04
Date of Event2019-12-04
Date Mfgr Received2019-12-04
Date Added to Maude2019-12-26
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 ContactMR. RICHARD YOUNGER
Manufacturer Street5818 EL CAMINO REAL
Manufacturer CityCARLSBAD CA 92008
Manufacturer CountryUS
Manufacturer Postal92008
Manufacturer Phone7604946842
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINVICTUS SPINAL FIXATION SYSTEM
Generic NameHXB
Product CodeHXB
Date Received2019-12-26
Model Number17001-01
Catalog Number1700-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALPHATEC SPINE INC
Manufacturer Address5818 EL CAMINO REAL CARLSBAD CA 92008 US 92008


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-12-26

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