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FDA 510(k) Applications Submitted by TINA LAKIN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K000262
01/28/2000
BOHN FEMORAL COMPONENT
BIOMET MANUFACTURING, INC.
K001010
03/29/2000
ASCENT KNEE REVISION FEMORAL STEM
BIOMET, INC.
K001580
05/22/2000
GROSS FEMORAL COMPONENT
BIOMET, INC.
K002757
09/05/2000
ONCOLOGY SALVAGE SYSTEM
BIOMET, INC.
K994007
11/24/1999
MALLORY/HEAD SMOOTH FEMORAL COMPONENT
BIOMET, INC.
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