To direct the U.S. military purchase of deployable external fixation g
ear, a project was designed to compare the biomechanical properties an
d ease of clinical application of military external fixators developed
by Synthes and Howmedica. The project assessed (a) ease of applicatio
n, (b) biomechanics, (c) heat stability, and (d) product line compatib
ility. Pretrained general surgery residents were provided with fresh c
adaver limbs with simulated grade IIIB tibial fractures and 5-cm middi
aphyseal defects. All chose the Howmedica Ultra-X for its ease of appl
ication but, on manual testing, noted that the Synthes Trauma-Fix was
more stable. The frames were biomechanically tested in a previously va
lidated model with strictly controlled parameters. The Howmedica Ultra
-X demonstrated only 75% of the compressive stiffness, 29% of the ante
roposterior bending stiffness, and 51% of the torsional stiffness of t
he Synthes Trauma-Fix. The Ultra-X failed to withstand steam steriliza
tion and was significantly weaker than, and incompatible with, Howmedi
ca's commercially available product. The Trauma-Fix demonstrated no st
atistically significant difference from Synthes' commercially availabl
e product. The Howmedica Ultra-X is unsuitable for military external f
ixation: The biomechanical properties are not equivalent to those of t
he unilateral Hoffmann frame, it is incompatible with commercially ava
ilable Howmedica external fixators, and it fails to withstand heat ste
rilization.