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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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