FDA 510(k) Applications Submitted by DANIEL A PONTECORVO

FDA 510(k) Number Submission Date Device Name Applicant
K172064 07/07/2017 Ti-Diagon Oblique TLIF Camber Spine Technologies
K193153 11/13/2019 SPIRA-C Integrated Fixation System Camber Spine Technologies
K133366 11/01/2013 ORTHROS POSTERIOR STABILIZATION SYSTEM CAMBER SPINE
K133529 11/15/2013 CAMBER SPINE COVERIS CERVICAL CAGE CAMBER SPINE
K134038 12/31/2013 CAMBER SPINE DIAGON OBLIQUE CAGE CAMBER SPINE
K203503 11/30/2020 Camber Sacroiliac (SI) Fixation System Camber Spine Technologies, LLC
K143490 12/08/2014 VERTA Corpectomy Cage CAMBER SPINE


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