InjuryHTG
UNKNOWN_RECONSTRUCTIVE_PRODUCT
Received Oct 9, 2013 · Event occurred Apr 25, 2011
Report 0002249697-2013-03226 · MDR key 3396733
Device
Product problems
- Insufficient Device Problem Information
Patient
81 YR
- No Code Available
Narrative
Description of Event or Problem
IT WAS REPORTED THAT THERE WAS A PATELLAR CREPITUS SYNDROME. ONLY POLY EXCHANGED.
Additional Manufacturer Narrative
CATALOGUE NUMBER UNKNOWN AT THIS TIME. DEVICE DESCRIPTION REPORTED AS UNKNOWN X3 POLYETHYLENE 8. ADDITIONAL INFORMATION HAS BEEN REQUESTED AND IF RECEIVED WILL BE SUBMITTED IN A FOLLOW UP REPORT UPON COMPLETION OF THE INVESTIGATION. DEVICE NOT RETURNED TO MANUFACTURER.