FDA 510(k) Applications Submitted by ROBERT R FRIDDLE

FDA 510(k) Number Submission Date Device Name Applicant
K070369 02/08/2007 REGENERX RINGLOC + MODULAR ACETABULAR SHELLS BIOMET, INC.
K101063 04/16/2010 SLEEVE WITH ZIPLOOP FIXATION DEVICES BIOMET SPORTS MEDICINE
K071395 05/21/2007 BIOMET VISION FOOTRING SYSTEM BIOMET MANUFACTURING CORP.
K083070 10/15/2008 TOGGLELOC SYSTEM BIOMET SPORTS MEDICINE
K103145 10/25/2010 HAMMERLOC TM TIBIAL FIXATION DEVICE BIOMET SPORTS MEDICINE
K080088 01/14/2008 BIOMET SPORTS MEDICINE ANCHOR DEVICES AND ZIPLOOP CONSTRUCTS BIOMET MANUFACTURING, INC.


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