InjuryHSH
IFORMA
Received Apr 20, 2011 · Event occurred Mar 1, 2011
Report 3004153240-2011-00020 · MDR key 2070966
Device
Generic name
Knee Interpositional Device
Catalog number
M57210600020
Product problems
- Insufficient Device Problem Information
Patient
49 YR
- No Code Available
Narrative
Additional Manufacturer Narrative
REVISION PLANNED FOR PATIENT WITH A KNEE INTERPOSITIONAL DEVICE. REVIEW OF THE DEVICE HISTORY RECORD INDICATED THAT THE DEVICE WAS MANUFACTURED TO SPECIFICATION. REVISION IS DUE TO PAIN CAUSED BY FEMOROPATELLAR ARTHRITIS UNRELATED TO THE IFORMA DEVICE.
Description of Event or Problem
REVISION PLANNED FOR PATIENT WITH A KNEE INTERPOSITIONAL DEVICE.