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FDA 510(k) Applications Submitted by ALLISON K KOSKEY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K052685
09/28/2005
ORTHOPEDIC SALVAGE SYSTEM- OSS
BIOMET, INC.
K052888
10/13/2005
POROUS TITANIUM ACETABULAR AUGMENTS
BIOMET MANUFACTURING CORP.
K052996
10/25/2005
POROUS TITANIUM ACETABULAR SHELLS
BIOMET MANUFACTURING CORP.
K052255
08/18/2005
ARCOMXL POLYETHYLENE RX90 ACETABULAR LINERS
BIOMET, INC.
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