InjuryHSH
IFORMA
Received May 3, 2011 · Event occurred Apr 1, 2011
Report 3004153240-2011-00024 · MDR key 2086541
Device
Generic name
Knee Interpositional Device
Catalog number
M57210600020
Product problems
- Insufficient Device Problem Information
Patient
54 YR
- No Code Available
Narrative
Additional Manufacturer Narrative
REVISION PLANNED FOR PT WITH A KNEE INTERPOSITIONAL DEVICE. REVIEW OF THE DEVICE HISTORY RECORD INDICATES THAT THE DEVICE WAS MFG TO SPECIFICATION.
Description of Event or Problem
REVISION PLANNED FOR PT WITH A KNEE INTERPOSITIONAL DEVICE.