inforMED
InjuryHSH

IFORMA

Received Nov 2, 2012 · Event occurred Jul 1, 2012

Report 3004153240-2012-00096 · MDR key 2833028

Device

Generic name

Knee Interpositional Device

Manufacturer

Conformis

Catalog number

M57210600010

Product problems

  • Appropriate Device Problem Term/Code Not Available

Patient

60 YR

  • No Information

Narrative

Description of Event or Problem

REVISION TO TKR PLANNED FOR PT WITH A KNEE INTERPOSITIONAL DEVICE.

Additional Manufacturer Narrative

REVISION TO TKR PLANNED FOR PT WITH A KNEE INTERPOSITIONAL DEVICE. REVIEW OF THE DEVICE HISTORY RECORD INDICATES THAT THE DEVICE WAS MANUFACTURED TO SPEC.