AVS TL SPACER 9 X 30 X 4 DEG 48370094

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 2020-03-13 for AVS TL SPACER 9 X 30 X 4 DEG 48370094 manufactured by Stryker Spine-us.

Event Text Entries

[184156480] Status of the device is unknown.
Patient Sequence No: 1, Text Type: N, H10


[184156481] It was reported that an avs tl spacer disengaged intra-operatively while attempting to insert at l4/5 level.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0009617544-2020-00038
MDR Report Key9829334
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-13
Date of Report2020-03-13
Date of Event2020-02-13
Date Mfgr Received2020-02-13
Date Added to Maude2020-03-13
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 NameAVS TL SPACER 9 X 30 X 4 DEG
Generic NameINTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR
Product CodeMAX
Date Received2020-03-13
Model Number48370094
Catalog Number48370094
Lot Number28429
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 2020-03-13

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