OASYS 3.5X26MM POLYAXIAL SCREW 48552326

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 2020-02-26 for OASYS 3.5X26MM POLYAXIAL SCREW 48552326 manufactured by Stryker Spine-us.

Event Text Entries

[184156875] Return status of the device is unknown.
Patient Sequence No: 1, Text Type: N, H10


[184156876] Stryker representative reported that during removal surgery, an oasys polyaxial screw head came off from main screw. No adverse consequences or medical intervention were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0009617544-2020-00030
MDR Report Key9759456
Report SourceHEALTH PROFESSIONAL
Date Received2020-02-26
Date of Report2020-02-26
Date of Event2020-01-29
Date Mfgr Received2020-01-29
Date Added to Maude2020-02-26
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. 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 NameOASYS 3.5X26MM POLYAXIAL SCREW
Generic NamePOSTERIOR CERVICAL SCREW SYSTEM
Product CodeNKG
Date Received2020-02-26
Model Number48552326
Catalog Number48552326
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
10 2020-02-26

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