FDA Adverse Event Other Summary report: N

UNI-KNEE TIBIA INSERT 9MM SIZE 3.4

MDR report key: 56442 · Received December 18, 1996

Report

Report Number
2935620-1996-00015
Event Type
Other
Date Received
December 18, 1996
Date of Event
November 13, 1996
Report Date
December 17, 1996
Manufacturer
INTERMEDICS ORTHOPEDICS, INC.
Product Code
HRY
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

NOTIFICATION OF DELAY IN SURGERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNI-KNEE TIBIA INSERT 9MM SIZE 3.4 Implant KNEE IMPLANT PROSTHESIS HRY INTERMEDICS ORTHOPEDICS, INC. NA 1232502

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Other 6100-00-130