FDA Adverse Event Injury Summary report: N

SUPERIOR END PLATE MEDIUM 6°-STERILE

MDR report key: 2944844 · Received February 5, 2013

Report

Report Number
2530088-2013-00103
Event Type
Injury
Date Received
February 5, 2013
Date of Event
January 1, 2010
Report Date
April 3, 2024
Manufacturer
BRANDYWINE
Product Code
MJO
UDI-DI
10705034700175
PMA / PMN Number
P050010
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
49530 SUPERIOR END PLATE MEDIUM 6°-STERILE PROSTHESIS, INTERVERTEBRAL DISC MJO BRANDYWINE 5372894 10705034700175

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention