FDA 510(k) Applications Submitted by TIBOR KOROS

FDA 510(k) Number Submission Date Device Name Applicant
K101609 06/08/2010 SELF RETAINING SOFT TISSUE RETRACTOR KOROS USA, INC.
K001915 06/23/2000 GRAFT MARKER RING T. KOROS SURGICAL INSTRUMENTS CORP.
K082399 08/20/2008 PECTUS STRUT KOROS USA, INC.
K002755 09/05/2000 NON-ABSORBING STERNATOMY MONOFILAMENT SUTURE T. KOROS SURGICAL INSTRUMENTS CORP.


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