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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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