Bonutti Research, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bonutti Research, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Bonutti Research, Inc. has 12 FDA 510(k) cleared orthopedic devices. Based in Effingham, US.
Historical record: 12 cleared submissions from 1999 to 2016.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bonutti Research, Inc.
12 devices
Cleared
Nov 10, 2016
JAS Pulse(TM) Ultrasonic Therapy
Physical Medicine
150d
Cleared
Jun 23, 2010
UNITY ULTRASONIC SYSTEM WITH PLLA ANCHORS
Orthopedic
266d
Cleared
Sep 10, 2009
UNITY BETA PLLA SYSTEM
Orthopedic
230d
Cleared
Oct 30, 2008
UNITY BETA ANCHOR SYSTEM
Orthopedic
30d
Cleared
Mar 15, 2007
UNITY ALPHA SYSTEM
Orthopedic
176d
Cleared
Feb 22, 2006
TRANSET SYSTEM
Orthopedic
19d
Cleared
Dec 16, 2005
MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM
Orthopedic
74d
Cleared
Feb 25, 2004
TRANSET FRACTURE FIXATION SYSTEM
Orthopedic
91d
Cleared
Dec 19, 2001
MULTITAK SUTURE SNAP SYSTEM
General & Plastic Surgery
86d
Cleared
Oct 29, 2001
MULTITAK SPLINTER 3.0 MM RESORBABLE ANCHOR
Orthopedic
89d
Cleared
May 08, 2001
MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR
Orthopedic
77d
Cleared
Dec 17, 1999
MULTITAK SS
Orthopedic
88d