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FDA 510(k) Applications Submitted by MARY LEWIS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970950
03/14/1997
EASY ROD
ACROMED CORP.
K981274
04/08/1998
ACROMED TIMX PLATE BASED LOW BACK SYSTEM
ACROMED CORP.
K981714
05/15/1998
TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM
ACROMED CORP.
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