FDA Adverse Event Other Summary report: N

CONSERVE TOTAL HEAD W/BFH

MDR report key: 1781262 · Received March 4, 2010

Report

Report Number
1043534-2010-00067
Event Type
Other
Date Received
March 4, 2010
Date of Event
December 14, 2009
Report Date
March 19, 2024
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Code
KWA
PMA / PMN Number
K021349
Report Source
Manufacturer report
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 1

DEVICE #2: INVESTIGATION IS NOT COMPLETE. TRENDS WILL BE EVALUATED. NO COMPLAINT WAS STATED AGAINST THIS PRODUCT. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETED. THIS IS THE SAME EVENT AS 1043534-2010-00066. THE EVENT OCCURRED IN (B)(6).

Description of Event or Problem · 1

.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONSERVE TOTAL HEAD W/BFH KWA WRIGHT MEDICAL TECHNOLOGY, INC. NA 08495582

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown