510(k) K072470

Device
BIOELAST 5-0 SUTURE, MODEL 500100
Applicant
Entrigue Surgical, Inc.
510(k) number
K072470
Product code
NWJ
Decision
Substantially Equivalent (SESE)
Decision date
2007-11-16
Date received
2007-09-04
Regulation
878.4494
Classification name
Suture, Recombinant Technology
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
GABRIELE NIEDERAUER
Address
3463 Magic Dr. Suite 320 San Antonio TX US 78229 78229

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K132348TEPHAFLEX BRAIDED SUTURETepha, Inc.2013-09-05
K130422PHANTOM FIBER BIOFIBER SUTURETornier, Inc.2013-04-04
K122487BIOFIBER SYTURETornier, Inc.2012-09-17
K100876AESCULAP MONOMAX ABSORBABLE SUTUREAesculap, Inc.2010-07-14
K082178TEPHAFLEX ABSORBABLE SUTURETepha, Inc.2008-10-30
K081099TEPHAFLEX ABSORBABLE SUTURETepha, Inc.2008-07-15
DEN060003TEPHAFLEX ABSORBABLE SUTURETepha, Inc.2007-02-08