FDA 510(k) Applications Submitted by SARA A BAILEY

FDA 510(k) Number Submission Date Device Name Applicant
K011451 05/11/2001 REUNITE FUSION SCREW BIOMET, INC.
K010657 03/06/2001 COPELAND MB RESURFACING HUMERAL HEADS BIOMET MANUFACTURING, INC.
K010664 03/06/2001 COPELAND RESURFACING HUMERAL HEADS BIOMET MANUFACTURING, INC.
K010827 03/20/2001 COPELAND MB/HA RESURFACING HUMERAL HEADS BIOMET ORTHOPEDICS, INC.
K011137 04/13/2001 RESORBABLE HAMMERTOE PIN BIOMET, INC.
K003044 09/29/2000 COPELAND RESURFACING HEADS BIOMET, INC.
K003253 10/17/2000 BIOMET'S MINIMALLY CONSTRAINED ELBOW BIOMET, INC.
K003493 11/13/2000 3I CALCIUM SODIUM PHOSPHATE BONE CEMENT BIOMET, INC.


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