MAGEC SPINAL BRACING AND DISTRACTION SYSTEM MC2-5590S

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 2020-02-27 for MAGEC SPINAL BRACING AND DISTRACTION SYSTEM MC2-5590S manufactured by Nuvasive Specialized Orthopedics, Inc..

Event Text Entries

[182914686] No product has been returned for evaluation as it will be returned to new castle engineering lab. Radiographs provided confirmed the alleged event. No root cause can be confirmed at this time.
Patient Sequence No: 1, Text Type: N, H10


[182914687] Information was received that x-ray images revealed that the end cap had disengaged from the rod. It is unknown if a revision procedure is planned. There was no patient injury reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006179046-2020-00119
MDR Report Key9765878
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-27
Date of Report2020-02-27
Date of Event2020-02-20
Date Mfgr Received2020-02-20
Device Manufacturer Date2018-06-25
Date Added to Maude2020-02-27
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 ContactMS. TIARA RAE
Manufacturer Street101 ENTERPRISE SUITE 100
Manufacturer CityALISO VIEJO CA 92656
Manufacturer CountryUS
Manufacturer Postal92656
Manufacturer G1NUVASIVE SPECIALIZED ORTHOPEDICS, INC.V
Manufacturer Street101 ENTERPRISE SUITE 100
Manufacturer CityALISO VIEJO CA 92656
Manufacturer CountryUS
Manufacturer Postal Code92656
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAGEC SPINAL BRACING AND DISTRACTION SYSTEM
Generic NameORTHOPEDIC INTERNAL FIXATION SYSTEMS, SPINAL
Product CodePGN
Date Received2020-02-27
Model NumberMC2-5590S
Lot Number8062511AAA
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNUVASIVE SPECIALIZED ORTHOPEDICS, INC.
Manufacturer Address101 ENTERPRISE SUITE 100 ALISO VIEJO CA 92656 US 92656


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-27

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