Mode Liste Mode Grille
Nom Classification Fabricant Classe de risque Pays Source
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall The HemiCAP Contoured Articular Prosthetic Orthopedic Devices Arthrosurface, Inc. 2 United States USFDA
Device Recall Arthrosurface ToeMotion" Orthopedic Devices Arthrosurface, Inc. Unclassified United States USFDA