FDA 510(k) Applications Submitted by JOHN WAGGONER

FDA 510(k) Number Submission Date Device Name Applicant
K960303 01/22/1996 FENNING FEMORAL COMPONENT BIOMET, INC.
K961021 03/14/1996 KIRSCHNER KNEE MODIFIED BIOMET, INC.
K961571 04/23/1996 COCR BI-ANGULAR HUMERAL COMPONENT BIOMET, INC.
K955350 11/21/1995 BIMETRIC COCR HEAD/NECK REPLACEMENT HIP STEM BIOMET, INC.


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