Captiva Spine’s MIS Pedicle Screw Systems Receive Additional FDA Clearance for Larger Diameter Pedicle Screws
Captiva Spine, Inc., announced today 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. - March 03, 2016
Captiva Spine’s SmartLOX™ Cervical Plate System Receives Clearance for Enhanced and Patented Screw Locking Mechanism
Captiva Spine's SmartLOX™ Cervical Plate System has received 510(K) clearance from the U.S. Food and Drug Administration (FDA) to market an enhanced cervical plate system with a patented screw locking mechanism. Their SmartLOX Cervical Plate System incorporates a proprietary Nitinol self-locking mechanism, which provides visual, audible, and tactile confirmation of the cervical screw locking. - July 21, 2015
Captiva Spine’s TowerLOX MIS Pedicle Screw System Receives Clearance for Enhanced Rod Insertion and Reduction
Captiva Spine, Inc., a medical device organization dedicated to creating and maintaining sincere, honest, collaborative relationships to deliver smart, elegant, and intuitive spinal solutions, announced today it has received 510(K) clearance from the U.S. Food and Drug Administration (FDA) to... - July 08, 2015
Captiva Spine’s Proprietary PivoRod® Articulating Minimally Invasive Spinal Rod Receives New U.S. Patent Allowance From US Patent Office
Captiva Spine, Inc., a medical device organization dedicated to developing and distributing spinal technologies in the US and internationally, announced today that a new U.S. patent has been allowed by the USPTO for Captiva Spine’s Proprietary PivoRod® Articulating Minimally Invasive... - October 03, 2013
Captiva Spine’s TowerLOX™ Minimally Invasive Pedicle Screw System Receives Clearance from FDA
Captiva Spine, Inc., a medical device organization dedicated to developing and distributing spinal technologies (in the U.S. and globally), today announced that it has received 510(k) clearance from the U.S. Food and Drug administration (FDA) to market the TowerLOX™ Minimally Invasive Lumbar Surgery System. - October 18, 2012
Captiva Spine® Broadens Product Offering with 510(k) Clearance for CapLOX II™ Spinal System
Captiva Spine, Inc., a medical device organization dedicated to developing and distributing spinal technologies in the US and internationally, today announced that it has received 510(k) clearance from the U.S. Food and Drug administration (FDA) to market the CapLOX II™ Spinal System, a... - September 15, 2011
Patents Awarded for Captiva Spine’s Proprietary Pivotec® Articulating Lumbar Interbody Fusion Device
Captiva Spine, Inc., a medical device organization dedicated to developing and distributing spinal technologies in the US and internationally, announced today that two new patents have been awarded by the USPTO for Captiva Spine’s Proprietary PIVOTEC® Articulating Lumbar Interbody Fusion... - August 16, 2011
Captiva Spine Acquires Proprietary Cervical Plate System, SmartLox™
Captiva Spine, Inc., a medical device organization dedicated to developing and distributing spinal technologies in the US and internationally, announced today that it has signed an agreement with Dr. Kamaljit Paul, Oshkosh, WI, to acquire the license to a Cervical Plate System designed and patented... - October 06, 2010
Captiva Spine Receives 510(k) Clearance for Its Proprietary Lumbar Interbody Fusion Device, the PIVOTEC™
Captiva Spine, Inc., a medical device organization dedicated to developing and distributing spinal technologies in the US and internationally, announced today that it has received 510(k) clearance for its cutting edge interbody system, the PIVOTEC™. Dale Mitchell, President and Founder of... - December 04, 2009