FDA 510(k) Applications Submitted by KLS MARTIN LP

FDA 510(k) Number Submission Date Device Name Applicant
K170124 01/13/2017 Level One Hand Plating System KLS MARTIN LP
K161259 05/04/2016 KLS Martin Cannulated Headless Screws KLS MARTIN LP
K161470 05/27/2016 Internal Distraction - Sterile KLS MARTIN LP
K173320 10/20/2017 KLS Martin L1 MMF System KLS Martin LP
K163315 11/23/2016 Internal Distraction - Sterile KLS Martin LP
K163579 12/20/2016 KLS Martin Individual Patient Solutions KLS Martin LP


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