European Program of Post-Authorization Safety Studies for Protelos®/Osseor® through EU-ADR Alliance

27/03/2015
02/07/2024
EU PAS number:
EUPAS9117
Study
Finalised
Documents
Study protocol
Initial protocol
English (1.61 MB - PDF) View document
Updated protocol
English (2.18 MB - PDF) View document
Study results
Study results
English (76.41 KB - PDF) View document
Study report
Other information