In a recent press release, Captiva Spine, Inc., announced that they have received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for larger diameter screws within their TowerLOX MIS Pedicle Screw System and CapLOX II Pedicle Screw System.
The additions to their systems include 8.5mm and 9.0mm Polyaxial Screws (non-cannulated, cannulated and reduction) for MIS, Mini-Open and Open cases in 30mm-100mm lengths, while maintaining all of the same instrument compatibilities to the implant. The expansion of Captiva Spine's line of cannulated and non-cannulated pedicle screws is an example of the company's promise to continuously provide improvements and enhanced capabilities on behalf of surgeons and patients, according to the release.
Dale Mitchell, President and Founder of Captiva Spine stated, "We are pleased to know that after successfully supporting over 5000 surgeries with Captiva Spine pedicle screws, that surgeons have come to know our company as providing thoughtful and elegant systems combined with reliable solutions for the growing and diverse clinical needs in spine care." During the recent introduction of the newest MIS rod inserters, Captiva Spine's Director of Research and Development, Dennis Ty, said "PivoQuik and PivoRod LP Inserters have been performing as expected, which has resulted in a bigger than expected demand for our reliable rod inserter tools and method." To continue reading, click here>>click here>>