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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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