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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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