For the treatment of bony defects in the skeleton, today there are fiv
e different options. Filling a defect by the application of autogenous
bone is one of them. Autogenous cancellous bone is still considered t
o be the gold standard, but numerous shortcomings of this material, de
scribed in detail in the paper, are not taken into account. Besides, w
e are still unable to influence bone healing by the transplantation of
autogenous bone with reference to quality, quantity of newly forming
bone and the time period, in which bone healing occurs. Investigation
into the different kinds of biomaterial developed to replace autogenou
s bone as a transplant, and their implantation into experimental anima
ls did not result in the production of a synthetic material that was:
as active as autogenous or even allogeneic cancellous bone. This was t
herefore not a solution to the problem. The reasons for this are multi
ple and are discussed in this paper. We developed a classification for
bone replacement materials that differentiates between biological, sy
nthetic, and composed materials, i.e., composite biomaterials made for
bone replacement. In reference to the literature, as well as our own
results, based on the implantation of more than 1200 rats, dogs and sh
eep with distinct materials, the plus/minus effects of the different c
lasses, groups and subgroups of bone replacement materials are summari
zed and discussed. The most recent knowledge about the mechanisms of b
one formation and how it is influenced by different growth factors, as
well as bioactive ceramics, indicates that in the future an applicabl
e bone replacement material will be a composite of a carrier material
combined with chemotactic, inductive, morphogenetic and proliferative,
chemically pure, recombinant factors, with a mainly local action. Unf
ortunately, the road to get there is long.