FDA Adverse Event Other Summary report: N

MENISCUS ARROW

MDR report key: 371340 · Received January 7, 2002

Report

Report Number
9613278-2001-00010
Event Type
Other
Date Received
January 7, 2002
Date of Event
May 29, 2001
Manufacturer
BIONX IMPLANTS LTD
Product Code
HRX
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MENISCUS ARROW BIOABSORBABLE SOFT TISSUE FIXATION DEVICE HRX BIONX IMPLANTS LTD 521110 1579

Patients

Seq Age Sex Outcome Treatment
1