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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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