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Corrective action for the AGC Dual Articular 2000 Knee Femoral Component, Biomet UK Ltd.

Product group Non-active implants - bone surgery
Reference 04161/15

For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.

Corrective action for the AGC Dual Articular 2000 Knee Femoral Component, Biomet UK Ltd. , Download_VeroeffentlichtAm_EN PDF, 2MB, File does not meet accessibility standards