FDA 510(k) Applications Submitted by PARADIGM SPINE

FDA 510(k) Number Submission Date Device Name Applicant
K213493 11/01/2021 Fortilink with TiPlus Technology Paradigm Spine
K080963 04/04/2008 DSS STABILIZATION SYSTEM PARADIGM SPINE
K071668 06/19/2007 ORTHOBIOM SPINAL SYSTEM PARADIGM SPINE


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