SutureTech's RapidFix earns FDA nod - Becker’s Spine Review

SutureTech earned FDA 510(k) clearance for its RapidFix device for soft tissue to bone fixation in orthopedic surgeries.

RapidFix is a suture-based internal fixation device and developed through eight years of surgeon collaboration, according to a Sept. 16 news release.

Following clearance, the company plans a limited market release of RapidFix in the fourth quarter.

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