FDA.reportPublic FDA data

MAUDE MDR 9908502

MDR report key
9908502
Report number
8030965-2020-02472
Event key
0
Event type
3
Date received
2020-03-31
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
1
Health professional
3
Initial report to FDA
3
Event location
3

Manufacturer Contact#

Contact
KARA DITTY-BOVARD
Address
EIMATTSTRASSE 3 OBERDORF 4436 SZ
Phone
610-610-6103
Report source
M
Manufacturer link flag
Y

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1UNK - SCREWS: CANNULATEDSCREW, FIXATION, BONEOBERDORF SYNTHES PRODUKTIONS GMBHHWCUNK - SCREWS: CANNULATED: TRAUR N

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12020-03-3101. R

Event Narratives#

No narrative records found.