BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Urgent Safety Notice for the AES Ankle prosthesis, Transystème

Product group Non-active implants - bone surgery
Reference 04810/12

The manufacturer Transystème informs about clinical follow-up for patients with AES Ankle prosthesis as occurrence of geodes may be observed around the tibial and talar component.

Urgent Safety Notice for the AES Ankle prosthesis, Transystème , Download_VeroeffentlichtAm_EN PDF, 352KB, File does not meet accessibility standards