Synthes (Usa) - FDA 510(k) Cleared Devices
411
Total
394
Cleared
0
Denied
Synthes (Usa) has 394 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 394 cleared submissions from 1977 to 2015.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
411 devices
Cleared
Mar 30, 2015
DEPUY SYNTHES VARIABLE ANGLE LOCKING HAND SYSTEM
Orthopedic
294d
Cleared
Mar 31, 2014
SYNTHES SYNSONIC ULNA NAIL
Orthopedic
276d
Cleared
Jul 06, 2012
SYNTHES 2.7/3.5MM VARIABLE ANGLE LCP ANKLE TRAUMA SYSTEM-ANTEROLATERAL DISTAL...
Orthopedic
35d
Cleared
Jun 18, 2012
SYNTHES VA LCP ANKLE TRAUMA SYSTEM
Orthopedic
89d
Cleared
May 08, 2012
SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM (MEDICAL AND POSTEROLATERAL DISTAL...
Orthopedic
61d
Cleared
Mar 21, 2012
SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM
Orthopedic
72d
Cleared
Feb 08, 2012
SET SCREW FOR TI TROCHANTERIC FIXATION NAIL(TFN)
Orthopedic
28d
Cleared
Dec 05, 2011
SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS
Orthopedic
174d
Cleared
Aug 08, 2011
SYNTHES 3.5MM LCP CLAVICLE PLATE SYSTEM
Orthopedic
67d
Cleared
Jul 28, 2011
SYNTHES STERNAL ZIPFIX SYSTEM
Orthopedic
128d
Cleared
Jul 25, 2011
3.7MM/5.0MM DYNAMIC LOCKING SCREW
Orthopedic
145d
Cleared
Apr 21, 2011
2.4 MM VA-LCP VOLAR RIM DISTAL RADIUS SYSTEM
Orthopedic
93d
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