FDA Adverse Event Other Summary report: N

DURAMATRIX

MDR report key: 1864585 · Received September 7, 2010

Report

Report Number
2249852-2010-00001
Event Type
Other
Date Received
September 7, 2010
Date of Event
July 2, 2010
Report Date
September 27, 2010
Manufacturer
COLLAGEN MATRIX, INC.
Product Code
GXQ
PMA / PMN Number
K040888
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PT REQUIRED REVISION SURGERY DUE TO CSF LEAKAGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DURAMATRIX COLLAGEN DURA SUBSTITUTE MEMBRANE GXQ COLLAGEN MATRIX, INC. CDSM33 0904101022

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention