UNKNOWN_SPINE_PRODUCT UNK_SPN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-10 for UNKNOWN_SPINE_PRODUCT UNK_SPN manufactured by Stryker Spine-us.

Event Text Entries

[178643776] Device remains implanted in patient.
Patient Sequence No: 1, Text Type: N, H10


[178643777] It was reported that 4 oasys occipital screws migrated 6 month post-operatively. The patient is experiencing pain. Revision surgery has not been planned at this time. This report represents the 2nd of the 4 screws.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004024955-2020-00002
MDR Report Key9689705
Report SourceHEALTH PROFESSIONAL
Date Received2020-02-10
Date of Report2020-02-10
Date of Event2020-01-13
Date Mfgr Received2020-01-13
Date Added to Maude2020-02-10
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. RITA KARAN
Manufacturer Street2 PEARL COURT
Manufacturer CityALLENDALE NJ 07401
Manufacturer CountryUS
Manufacturer Postal07401
Manufacturer Phone2017608000
Manufacturer G1STRYKER SPINE-FRANCE
Manufacturer StreetZONE INDUSTRIELLE DE MARTICOT
Manufacturer CityCESTAS 33610
Manufacturer CountryFR
Manufacturer Postal Code33610
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN_SPINE_PRODUCT
Generic NamePOSTERIOR CERVICAL SCREW SYSTEM
Product CodeNKG
Date Received2020-02-10
Catalog NumberUNK_SPN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER SPINE-US
Manufacturer Address2 PEARL COURT ALLENDALE NJ 07401 US 07401


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-10

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