FDA Adverse Event Injury Summary report: N

RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

MDR report key: 195069 · Received November 4, 1998

Report

Report Number
2184002-1998-00756
Event Type
Injury
Date Received
November 4, 1998
Date of Event
September 21, 1998
Report Date
November 4, 1998
Manufacturer
LIFECORE BIOMEDICAL, INC.
Product Code
DZE
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
DENTIST

Narratives

Description of Event or Problem · 1

IMPLANT PLACED 3/25/1997. IT FAILED AND WAS REMOVED 9/21/1998.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT Implant ENDOSSEOUS IMPLANT DZE LIFECORE BIOMEDICAL, INC. R9010-50-10 75960409

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Required Intervention