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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