Tornier, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Tornier Perform™ Reversed Monopost Glenoid (Perform Mono), Tornier Humeral Reconstruction System Max (Tornier HRS Max), Tornier Humeral Nail and Tornier Long Humeral Nail
51
Total
51
Cleared
0
Denied
FDA 510(k) Regulatory Record - Tornier, Inc. General & Plastic Surgery ✕
5 devices
Cleared
Apr 04, 2013
PHANTOM FIBER BIOFIBER SUTURE
General & Plastic Surgery
43d
Cleared
Sep 17, 2012
BIOFIBER SYTURE
General & Plastic Surgery
33d
Cleared
Jan 25, 2012
TORNIER COLLAGEN COATED BIOFIBER SCAFFOLD
General & Plastic Surgery
258d
Cleared
May 10, 2011
TORNIER BIOFIBER SCAFFOLD
General & Plastic Surgery
228d
Cleared
Apr 22, 2010
TORNIER SURGICAL MESH
General & Plastic Surgery
133d