FDA Adverse Event Injury Summary report: N

1221934-2012-00337

MDR report key: 2866174 · Received December 10, 2012

Report

Report Number
1221934-2012-00337
Event Type
Injury
Date Received
December 10, 2012
Report Date
November 27, 2012
Manufacturer
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
PMA / PMN Number
K102298
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER
Health Professional
N

Patients

Seq Age Sex Outcome Treatment
1 NA Male NA.