FDA 510(k) Applications Submitted by Captiva Spine, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K193270 11/26/2019 CapLOX II«/TowerLOX« MIS Pedicle Screw System Captiva Spine, Inc.
K180475 02/22/2018 CapLOX II« / TowerLOX« MIS Pedicle Screw System Captiva Spine, Inc.
K180990 04/16/2018 TirboLOX-L Lumbar IBFD Captiva Spine, Inc.
K181229 05/09/2018 TirboLOX-C Cervical IBFD Captiva Spine, Inc.


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