FDA 510(k) Applications Submitted by BONUTTI RESEARCH, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K090175 01/23/2009 UNITY BETA PLLA SYSTEM BONUTTI RESEARCH, INC.
K060283 02/03/2006 TRANSET SYSTEM BONUTTI RESEARCH, INC.
K010479 02/20/2001 MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR BONUTTI RESEARCH, INC.
K012465 08/01/2001 MULTITAK SPLINTER 3.0 MM RESORBABLE ANCHOR BONUTTI RESEARCH, INC.
K993115 09/20/1999 MULTITAK SS BONUTTI RESEARCH, INC.
K013177 09/24/2001 MULTITAK SUTURE SNAP SYSTEM BONUTTI RESEARCH, INC.
K052799 10/03/2005 MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM BONUTTI RESEARCH, INC.
K062820 09/20/2006 UNITY ALPHA SYSTEM BONUTTI RESEARCH, INC.
K082906 09/30/2008 UNITY BETA ANCHOR SYSTEM BONUTTI RESEARCH, INC.
K093078 09/30/2009 UNITY ULTRASONIC SYSTEM WITH PLLA ANCHORS BONUTTI RESEARCH, INC.
K033717 11/26/2003 TRANSET FRACTURE FIXATION SYSTEM BONUTTI RESEARCH, INC.
K161628 06/13/2016 JAS Pulse(TM) Ultrasonic Therapy Bonutti Research, Inc.


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