INBONE Technologies, Inc. Launches New Expanded Fusion Clinical Study

BERKELEY, Calif.--(BUSINESS WIRE)--Nine surgeons from across the country have agreed to participate in a new expanded clinical study for the INBONE™ Fusion System. These surgeons come from both private and university hospitals, such as Duke, UCLA, and Yale. The INBONE Fusion system was cleared by The FDA 510(k) in July of 2005. Since then over 100 fusion cases have been completed using the system. Early results have shown an accelerated fusion rate to an average 4-8 week timeframe with non union rates at a very low 2%. That fusion time is approximately twice as fast as traditional plates and screws and approximately one-tenth of the failure rate of traditional methods.

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