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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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