The Food and Drug Administration granted 14 spine device-related clearances in April, according to an FDA report.

The Food and Drug Administration granted 33 orthopedic- and spine-related device clearances in April.

The Food and Drug Administration granted 17 spine-related medical device clearances in March.

Biotechnology company Arteriocyte has received approval from the Food and Drug Administration to initiate a Phase I clinical trial with its Magellan MAR01 technology for treating compartment syndrome in extremity trauma patients.

The Food and Drug Administration granted 38 orthopedic- and spine-related medical device clearances in March.

Ascendx Spine announced it received FDA 510(k) clearance for its Acu-Cut Vertebral Augmentation System for treating vertebral compression fractures.

The Food and Drug Administration granted 17 spine-related device clearances in February.

The Food and Drug Administration granted 44 orthopedic- and spine-related 510(k) clearances in February, according to an FDA report.

Surgeons from Sinai Hospital, part of LifeBridge Health, recently used the first externally controllable internal limb lengthening device with FDA clearance, the PRECICE Limb Lengthening System, which they helped co-develop, according to a LifeBridge news release.

The Food and Drug Administration granted 19 spine-related device clearances in January, according to an FDA report.