FDA 510(k) Applications Submitted by VIKKI M O'CONNOR

FDA 510(k) Number Submission Date Device Name Applicant
K090166 01/22/2009 AVS ANTERIOR LARGE PEEK SPACERS STRYKER CORP.
K080758 03/18/2008 AVS PL PEEK SPACERS, MODELS 48351 AND 48353 STRYKER CORP.
K090816 03/25/2009 STRYKER SPINE AVS PL PEEK SPACERS STRYKER CORP.
K090885 03/31/2009 NEPHROS, INC., DSU DUAL STAGE ULTRAFILTER NEPHROS, INC.
K082014 07/15/2008 STRYKER SPINE AVS PL PEEK SPACERS STRYKER CORP.


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