CoNextions Gets 510(k) Clearance for Tenodesis System

March 17, 2020

CoNextions has received 510(k) clearance from the FDA for its Coronet system, a tenodesis product designed for tissue-to-bone and tissue-to-tissue attachment.

The company said that its implant, which is used for tendon repairs, provides enhanced fixation strength compared to conventional suture repairs.

CoNextions plans to begin marketing the system in the U.S. during the second quarter of 2020.

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