InjuryHSH
IFORMA
Received Nov 2, 2012 · Event occurred Sep 1, 2012
Report 3004153240-2012-00098 · MDR key 2833027
Device
Product problems
- Insufficient Device Problem Information
Patient
59 YR
- No Information
Narrative
Description of Event or Problem
REVISION TO TER 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 SPECIFICATION.