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FDA 510(k) Applications Submitted by Mireille Lemery
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060209
01/27/2006
AEQUALIS SHOULDER FRACTURE SYSTEM & AEQUALIS SHOULDER SYSTEM
TORNIER
K050316
02/09/2005
AEQUALIS REVERSED SHOULDER PROSTHESIS
TORNIER
K060438
02/21/2006
RHS
TORNIER
K060545
03/01/2006
UNITY HUMERAL PLATE
TORNIER
K070787
03/22/2007
LATITUDE ELBOW PROTHESIS
TORNIER
K050848
04/04/2005
TORNIER ELBOW PROSTHESIS
TORNIER
K031218
04/17/2003
MODIFICATION TO TORNIER TOTAL ELBOW PROSTHESIS
TORNIER
K041339
05/20/2004
AEQUALIS SHOULDER SYSTEM
TORNIER
K161414
05/23/2016
Anatomic Total Knee System
AMPLITUDE
K061439
05/24/2006
AEQUALIS REVERSED PROSTHESIS
TORNIER
K061824
06/28/2006
TORNIER CEMENT RESTRICTOR
TORNIER
K032079
07/07/2003
HLS NOETOS SYSTEM
TORNIER
K022211
07/08/2002
HLS UNI EVOLUTION PROSTHESIS
TORNIER
K041873
07/12/2004
AEQUALIS REVERSED SHOULDER PROSTHESIS
TORNIER
K071948
07/13/2007
AEQUALIS REVERSED ADAPTER
TORNIER
K062661
09/07/2006
AEQUALIS RESURFACING HEAD
TORNIER
K063081
10/10/2006
AEQUALIS SHOULDER SYSTEM
TORNIER
K063551
11/24/2006
AEQUALIS HUMERAL PLATE
TORNIER
K013906
11/26/2001
HLS NOETOS SYSTEM
TORNIER
K133777
12/12/2013
TORNIER INSITE(TM) FT PEEK KNOTLESS SUTURE ANCHOR
TORNIER, INC.
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