Acuitive Technologies this week announced that it received FDA 510(k) clearance for its Citrespline and Citrelock ligament reconstruction devices. The two systems are designed to firmly engage tendons and ligaments with a bone tunnel while preserving the integrity of the soft tissue during insertion of the device, according to the company. Citrespline and Citrelock are […]
Acuitive Technologies
Acuitive Technologies knotless suture anchor wins FDA clearance
Acuitive Technologies yesterday said it received FDA 510(k) clearance for its Citregen knotless suture anchor. Citrefix is designed to assist in the attachment of tissue to the bone during orthopedic surgeries, such as fixation of ligaments or tendon graft tissue repairs of the shoulder, elbow, wrist, hand, knee, ankle and foot extremities. “This FDA clearance […]
Acuitive Technologies wins FDA clearance for tendon interference screw system
Acuitive Technologies announced today that it received FDA 510(k) clearance for its CitreLock interference screw system. CitreLock with CitreGen material technology, a next-generation thermoset bioresorbable synthetic polymer, is designed to attach tissue during orthopedic surgeries, including the fixation of ligaments or tendon graft tissue repairs of the shoulder, elbow, wrist, hand, knee and foot extremities, […]
