FDA.reportPublic FDA data

MAUDE MDR 8962413

MDR report key
8962413
Report number
8962413
Event key
0
Event type
3
Date of event
2019-08-15
Date received
2019-09-04
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
500
Health professional
3
Initial report to FDA
3
Event location
3

Manufacturer Contact#

Report source
U
Manufacturer link flag
N

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1COMPONENTS, WHEELCHAIRUNKKNN* *

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12019-09-040

Event Narratives#

No narrative records found.