STAPLE, FIXATION, BONE

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 2020-03-25 for STAPLE, FIXATION, BONE manufactured by Crossroads Extremity Systems.

MAUDE Entry Details

Report Number3011421599-2020-00005
MDR Report Key9880257
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-25
Date Added to Maude2020-03-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer Street6055 PRIMACY PARKWAY STE 140
Manufacturer CityMEMPHIS, TN
Manufacturer CountryUS
Manufacturer Phone2218406
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Generic NameSTAPLE, FIXATION, BONE
Product CodeJDR
Date Received2020-03-25
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCROSSROADS EXTREMITY SYSTEMS
Manufacturer Address6055 PRIMACY PARKWAY STE 140 MEMPHIS, TN US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-25

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