FDA 510(k) Applications Submitted by VICTORIA SCHEITLIN

FDA 510(k) Number Submission Date Device Name Applicant
K140625 03/11/2014 ORTHOSORB LS BIOMET, INC.
K140891 04/08/2014 BIOMET CANNULATED SCREW SYSTEM BIOMET, INC.
K152241 08/10/2015 Medtronic Transportation/Sterilization Cassettes Medtronic Sofamor Danek USA, Inc.
K152338 08/19/2015 VERTEX(r) Reconstruction System MEDTRONIC SOFAMOR DANEK USA, INC
K142658 09/18/2014 Biomet Headless Compression and Twist-off Screws BIOMET MANUFACTURING CORP.
K143188 11/05/2014 3.Omm Biomet Cannulated Screw System BIOMET MANUFACTURING CORP.


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