FDA.reportPublic FDA data

MAUDE MDR 9884535

MDR report key
9884535
Report number
2031966-2020-00058
Event key
0
Event type
3
Date of event
2019-07-05
Date received
2020-03-26
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
MISS VIRNALISA COBACHA
Address
7475 LUSK BLVD SAN DIEGO CA 92121 US
Report source
M
Manufacturer link flag
Y

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1NUVASIVE BASE INTERFIXATED TITANIUM SYSTEMINTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, LUMBARNUVASIVE, INCORPORATEDOVDR N

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12020-03-2601. O

Event Narratives#

No narrative records found.