GLENOSPHERE - 32MM DIA X 2MM THK CONCENTRIC 5573-C-3202

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 2020-03-17 for GLENOSPHERE - 32MM DIA X 2MM THK CONCENTRIC 5573-C-3202 manufactured by Stryker Gmbh.

MAUDE Entry Details

Report Number0008031020-2020-00733
MDR Report Key9845749
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-17
Date of Report2020-03-17
Date of Event2020-02-24
Date Mfgr Received2020-02-24
Date Added to Maude2020-03-17
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. KEVIN SMITH
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1STRYKER ORTHOPAEDICS-MAHWAH
Manufacturer Street325 CORPORATE DRIVE
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal Code07430
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGLENOSPHERE - 32MM DIA X 2MM THK CONCENTRIC
Generic NamePROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
Product CodeKWS
Date Received2020-03-17
Model Number5573-C-3202
Catalog Number5573-C-3202
Lot Number5Y1R46
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER GMBH
Manufacturer AddressBOHNACKERWEG 1 POSTFACH SELZACH 2545 CH 2545


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-03-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.