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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