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FDA 510(k) Applications Submitted by ENTRIGUE SURGICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K072470
09/04/2007
BIOELAST 5-0 SUTURE, MODEL 500100
ENTRIGUE SURGICAL, INC.
K130354
02/12/2013
MEDIENT MIDDLE TURBINATE IMPLANT; (SINGLE PACK-1 PAIR, FOUR PACK-4 PAIR)
ENTRIGUE SURGICAL, INC.
K082750
09/19/2008
ENTACT SEPTAL STAPLER, MODEL 610-00100
ENTRIGUE SURGICAL, INC.
K121351
05/04/2012
SINUS DILATION SYSTEM
ENTRIGUE SURGICAL, INC.
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