Synthes Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synthes Spine - FDA 510(k) Cleared Devices
36
Total
32
Cleared
0
Denied
Synthes Spine has 32 FDA 510(k) cleared orthopedic devices. Based in Paoli, US.
Historical record: 32 cleared submissions from 1995 to 2012.
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 - Synthes Spine
36 devices
Cleared
Dec 17, 2012
SYNTHES NAVIGABLE PEDICLE PREPARATION INSTRUMENTS
Neurology
145d
Cleared
Jul 31, 2012
SYNTHES MATRIX SYSTEM
Orthopedic
133d
Cleared
Jun 14, 2012
SYNTHES SCOUT TACK FIXATION
Orthopedic
426d
Cleared
May 18, 2012
SYNTHES MATRIX SYSTEM
Orthopedic
52d
Cleared
May 14, 2012
SYNTHES USS CONNECTOR
Orthopedic
77d
Cleared
Feb 01, 2012
SYNTHES USS CONNECTORS
Orthopedic
100d
Cleared
Dec 21, 2011
SYNTHES MIRS
Orthopedic
70d
Cleared
Nov 18, 2011
SYNTHES USS
Orthopedic
186d
Cleared
Feb 18, 2011
SYNTHES SCOUT VESSEL GUARD
Cardiovascular
78d
Cleared
Jan 05, 2011
SYNTHES 6.0 COCR AND CPT TI-3 RODS
Orthopedic
65d
Cleared
Dec 20, 2010
SYNTHES ZERO-P
Orthopedic
378d
Cleared
Aug 05, 2010
MODIFICATION TO SYNTHES MATRIX SYSTEM
Orthopedic
121d