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Strong IDE results with favorable safety/effectiveness signals and a clear regulatory pathway potential could drive near-term upside risk/reward for ABT, though ultimate earnings impact awaits FDA approval and commercial rollout.
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Abbott reported strong 30-day results from the TECTONIC CAD IVL IDE study for the SonicForce Coronary IVL System, meeting safety and efficacy endpoints. The trial enrolled 335 patients across 40 U.S. sites and showed a 0.3% 30-day target lesion failure, 97% procedural success, and 0.3% MACE, with OCT imaging confirming calcium fractures and improved post-stent expansion. A potential FDA pathway could broaden Abbott's complex-CAD toolkit.
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