InjuryHSH
IFORMA
Received Oct 18, 2011 · Event occurred Jan 1, 2008
Report 3004153240-2011-00042 · MDR key 2304628
Device
Product problems
- Insufficient Device Problem Information
Patient
52 YR
- No Code Available
Narrative
Description of Event or Problem
PT WITH A KNEE INTERPOSITIONAL DEVICE WAS REVISED TO A UNICONDYLAR KNEE IMPLANT.
Additional Manufacturer Narrative
PT WITH A KNEE INTERPOSITIONAL DEVICE WAS REVISED TO A UNICONDYLAR KNEE IMPLANT. REVIEW OF THE DEVICE HISTORY RECORD INDICATES THAT THE DEVICE WAS MANUFACTURED TO SPECIFICATION.