Home » SeaSpine Gets 510(k) Clearance for Spinal Surgery Module
SeaSpine Gets 510(k) Clearance for Spinal Surgery Module
July 9, 2021
Carlsbad, Calif.-based SeaSpine Holdings has received 510(k) clearance from the FDA for its 7D Percutaneous Spine Module for use in minimally invasive surgery.
The camera-based system uses algorithms to create a 3D image for surgical navigation, which is intended to lead to shorter and more efficient spinal procedures.
SeaSpine, which specializes in surgical solutions for spinal disorders, says the new application offers increased functionality for its 7D Flash Navigation System.
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