Tornier - FDA 510(k) Cleared Devices
44
Total
44
Cleared
0
Denied
Tornier has 44 FDA 510(k) cleared orthopedic devices. Based in Concord, US.
Historical record: 44 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.
44 devices
Cleared
Mar 13, 2012
AEQUALIS SHOULDER FRACTURE SYSTEM, AEQUALIS REVERSED SHOULDER PROSTHESIS,...
Orthopedic
231d
Cleared
Feb 23, 2012
KNEETEC PFJ&HLS KNEETEC PATELLAR COMPONENT
Orthopedic
227d
Cleared
Nov 03, 2011
AEQUALIS SHOULDER SYSTEM
Orthopedic
121d
Cleared
May 05, 2011
HLS KNEETEC SYSTEM
Orthopedic
492d
Cleared
May 06, 2010
AEQUALIS REVERSED SHOULDER PROSTHESIS
Orthopedic
107d
Cleared
Sep 21, 2009
TORNIER, PITON FIXATION IMPLANT SYSTEM
Orthopedic
90d
Cleared
Mar 17, 2009
SALTO TALARIS TOTAL ANKLE PROSTHESIS
Orthopedic
64d
Cleared
Jan 27, 2009
AEQUALIS HUMERAL NAIL SYSTEM
Orthopedic
130d
Cleared
Oct 24, 2008
AEQUALIS REVERSED FRACTURE SHOULDER PROTHESIS
Orthopedic
88d
Cleared
Jul 17, 2008
AEQUALIS REVERSED SHOULDER PROSTHESIS
Orthopedic
94d
Cleared
Oct 18, 2007
AEQUALIS REVERSED ADAPTER
Orthopedic
97d
Cleared
Aug 24, 2007
LATITUDE ELBOW PROTHESIS
Orthopedic
155d
Looking for a specific device from Tornier? Search by device name or K-number.
Search all Tornier devices