NONE UNK NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00 report with the FDA on 2014-11-20 for NONE UNK NA manufactured by Nuvasive, Inc..

Event Text Entries

[15124113] Following implantation of a single-level interbody implant and unilateral posterior fixation on (b)(6) 2012, paralysis was reported to have occurred. No specific information related to the chain of events leading up to the injury are known. No specific allegations have been made regarding a product failure that resulted in the injury.
Patient Sequence No: 1, Text Type: D, B5


[15257683] (b)(4). No device have been returned and no evaluation can be completed. No information about the event or the injury has been received. No further investigation can be completed at this time.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2031966-2014-00077
MDR Report Key4548707
Report Source00
Date Received2014-11-20
Date of Report2014-11-20
Date of Event2012-10-17
Date Mfgr Received2014-10-20
Date Added to Maude2015-02-26
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 FDA0
Event Location0
Manufacturer ContactPAUL HOLBROOK
Manufacturer Street7475 LUSK BLVD
Manufacturer CitySAN DIEGO CA 92121
Manufacturer CountryUS
Manufacturer Postal92121
Manufacturer Phone8583205285
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNONE
Generic NameNONE
Product CodeJDN
Date Received2014-11-20
Model NumberUNK
Catalog NumberNA
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNUVASIVE, INC.
Manufacturer Address7475 LUSK BLVD SAN DIEGO CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Deathisabilit 2014-11-20

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