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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